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  1. Animal Drug Compounding

Bulk Drug Substances Reviewed and Not Listed

List of Bulk Drug Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals

List of Bulk Drug Substances for Compounding Drugs for Use in Food-Producing Animals or Free-Ranging Wildlife Species

Bulk Drug Substances Currently Under Review


FDA reviewed these bulk drug substances and is not including them on either 1) The List of Bulk Drug Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals, or 2) The List of Bulk Drug Substances for Compounding Drugs for Use in Food-Producing Animals or Free-Ranging Wildlife Species. Therefore, these bulk drug substances are not covered by the enforcement discretion policy described in Guidance for Industry #256 Compounding Animal Drugs from Bulk Drug Substances. These substances may be nominated again for re-evaluation by FDA using the nomination procedure described in the appendix to GFI #256.

FDA will accept nominations of additional bulk drug substances at any time and will continue to review nominations and update lists. For information on how to submit a bulk drug substance nomination, see the appendix to Guidance for Industry #256 Compounding Animal Drugs from Bulk Drug Substances.

DOGS, CATS, HORSES

Bulk Drug Substance (BDS) Species Dosage form(s) Strength/concentration Reason
Amikacin
(3/8/2023)
dog, cat



dog, cat, horse
otic ointment

otic solutions

injectable solution
0.67% - 5%

0.67% - 5%

200mg/mL
There are several FDA-approved otic products that could be used as labeled in an urgent situation. If a compounded preparation of amikacin is needed, a patient-specific prescription should suffice. 

If an injectable solution is needed for urgent treatment, Amiglyde-V® (NADA 127-892) or the amikacin injectable solutions FDA-approved for use in humans can be used in an extralabel manner under 21 CFR Part 530.
Amlodipine besylate
(1/19/2023)
dog, cat oral solution

oral suspension

capsule

transdermal gel

oral paste

tablet

soft chewable treat
any concentration other than 1.25 mg/ml
any concentration other than 1.25 mg/ml
any strength other than 0.625 mg
any concentration

any concentration

any strength other than 0.625 mg
any strength 
Insufficient rationale was provided for the need for transdermal gel, oral paste, and soft chewable treat dosage forms on an urgent basis and specialty formulations can be obtained via patient-specific prescription and are not generally needed as office stock; insufficient rationale was provided for the needs of strengths other than 0.625 mg for capsules and tablets or for concentrations other than 1.25 mg/mL for oral solutions and oral suspensions as office stock to be used on an urgent basis.  
Apomorphine hydrochloride
(8/11/2016)
dog subconjunctival solution
subconjunctival tablets

3.125-6.25 mg/mL

6.25 mg

Clevor (ropinirole ophthalmic solution) 30 mg/mL (NADA 141-534) is now FDA-approved for induction of emesis in dogs.
Azithromycin dog, cat, horse




dog, cat
capsule
liquid
tablet, flavored or unflavored
otic
ointment/solution

oral paste
oral powder
mucoadhesive paste
periodontal gel
soft chew treat
10 – 500 mg
1 – 250 mg/ml
25 – 50 mg
225 mg
0.5 – 5%

20 – 360 mg/ml
1 gm/dose
100 mg/ml
8.5%
25 – 200 mg
There are many FDA-approved and marketed antibiotics that can be used in an urgent situation in dogs, cats, and horses. If a compounded preparation of azithromycin is needed, a patient specific prescription should suffice.
Betamethasone dipropionate
(3/29/2023)
dog, cat, horse otic ointment 
otic suspension
0.05% - 1%
0.05% - 1%
There are several FDA-approved and marketed steroid-containing otic products, with and without antibiotics and/or antifungals, labeled for use in dogs and cats, which can also be used in an extralabel manner in horses. If a compounded preparation of betamethasone is needed, a patient-specific prescription should suffice.
Buprenorphine 
HCl
(4/24/2023)
dog, horse


dog, cat, horse
injectable 
polymeric matrix 
solution

injectable solution

oral solution
any



any

any
FDA-approved injectable solution is available as labeled for administration or for extralabel use under 21 CFR Part 530 for injection or oral administration. Specialty formulations can be obtained via patient-specific prescription and are not generally needed as office stock.
Chloramphenicol
(2/28/2023)
horse powder for oral administration

topical ointment

ophthalmic solution or ointment
10 g

1%

1%
Oral suspension and paste are listed on the List of Bulk Drug Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals for use in horses. For topical and ophthalmic use, there are FDA-approved human and animal drug products available for initial empirical treatment, there are human health risks associated with administration of chloramphenicol, and in instances where chloramphenicol may be indicated based on culture and sensitivity results, this preparation can be compounded on an individual patient basis and is not needed for urgent or immediate treatment to prevent animal suffering or death.
Chloramphenicol
(2/28/2023)
dog, cat capsule

oral suspension

otic ointment/solution/suspension
30 - 1000 mg

125 - 500 mg/mL

1 - 2%
There are FDA-approved animal drug products available for initial empirical treatment. In instances where chloramphenicol may be indicated based on culture and sensitivity results, this preparation can be compounded on an individual patient basis and is not needed for urgent or immediate treatment to prevent animal suffering or death.
Clenbuterol
(6/6/2023)
horse oral solution any Ventipulmin Syrup, NADA 140-973, is FDA-approved and can be used as labeled, or in an extralabel manner under 21 CFR Part 530, in horses in an urgent situation, until a patient-specific prescription can be filled, if needed.
Corticotropin (ACTH)
(1/19/2023)
dog, cat, horse injectable 40 & 80 units/ml There are FDA-approved products that can be used in an extralabel manner under 21 CFR Part 530 in dogs, cats, and horses. There is lack of supporting information that this drug is needed on an urgent basis in these species.
Dexamethasone
(9/21/2016)
horse oral powder 10 mg/packet FDA-approved human oral tablets can be used to compound 10 mg oral powder doses.
Dipyrone
(10/5/2016)
Shar-Pei and Shar-Pei mixed breed dogs solution for injection 250 and 500 mg/ml The FDA-approved drug product Zimeta (dipyrone 500 mg/mL) (NADA 141-513) can be used in an extralabel manner under 21 CFR part 530.
Enrofloxacin
(9/21/2016)
horse oral paste and suspension 100-200 mg/ml There are FDA-approved enrofloxacin products that can be used in an extralabel manner or used to compound enrofloxacin paste and suspension.
Famciclovir
(6/6/2023)
cat capsules
oral paste
oral powder
soft chew treats
unflavored tablets
flavored quadrisected tablet

oral suspension
any






any, other than 25-325 mg/ml
Famciclovir in an oral suspension (25 - 325 mg/ml) for cats is on the List of Bulk Drug 
Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals. In 
addition, FDA-approved famciclovir tablets can be used in an extralabel manner under 21 CFR 
Part 530 to treat the same conditions in cats.
Flumethasone
(4/18/2023)
horse injectable solution any FDA-approved Bimasone (ANADA 200-612) can be used in horses in an urgent situation until a patient-specific prescription for another dosage form can be filled, if needed.
Fluoxetine
(12/21/2022)
dog, cat, horse capsule, tablet, soft chew treat, suspension, paste, transdermal gel all strengths and concentrations Fluoxetine may take several weeks to achieve a therapeutic effect and is not needed for urgent treatment to avoid animal suffering or death. Reconcile® (fluoxetine), NADA 141-272, is approved for use in dogs and there are alternative medications FDA-approved for use in animals that could be used to treat some of the nominated conditions. Additionally, fluoxetine products FDA-approved for use in humans can be used in an extralabel manner if deemed appropriate by a veterinarian as could several other alternative drugs FDA-approved for use in humans. If fluoxetine is needed in a formulation that is not FDA-approved, a patient-specific prescription for compounded fluoxetine should be sufficient.
Flurbiprofen
(3/29/2023)
dog, cat ophthalmic suspension 0.04% FDA-approved flurbiprofen ophthalmic products for humans can be used in an extralabel manner under 21 CFR Part 530 to treat dogs and cats in an urgent situation, until a patient-specific prescription can be filled, if needed.
Gentamicin
(3/29/2023)
dog, cat otic ointment
otic solution
anal sac ointment
topical gel
topical ointment
otic ointment
otic suspension
ophthalmic ointment
0.3-1%
0.3-1%
0.3-1%
0.3%
0.3%
0.3%
0.3%
0.3%
FDA-approved and marketed combination drug products containing gentamicin or other drugs can be used as labeled in an urgent situation in dogs and cats. Drugs containing gentamicin approved for other animal species and humans that be used in an extralabel manner under 21 CFR Part 530. If a compounded preparation of gentamicin is needed, a patient-specific prescription should suffice.
Isoflupredone acetate
(12/6/2022)
horse suspension for injection 2 mg/ml FDA-approved drugs are available for urgent use in horses for the same or similar indications.
Ketoconazole/amikacin sulfate/triamcinolone acetonide
(2/28/2023)

Ketoconazole/chloramphenicol/triamcinolone acetonide
(2/28/2023)

Ketoconazole/enrofloxacin/triamcinolone acetonide
(2/28/2023)

Ketoconazole/gentamicin/triamcinolone acetonide
(2/28/2023)

Ketoconazole/mupirocin/triamcinolone acetonide
(2/28/2023)

Ketoconazole/ofloxacin/triamcinolone acetonide
(2/28/2023)
dog, cat otic gel
otic suspension
otic solution
otic ointment
any There are many FDA-approved and marketed otic combination drug products that can be used as labeled in an urgent situation in dogs and cats. If a compounded preparation of this otic combination is needed, a patient-specific prescription should suffice.
maropitant citrate
(1/20/2023)
dog, cat capsules

oral paste

oral suspension

soft chew treat

tablet, flavored, quadrisected

transdermal gel

nasal solution 

2 – 120 mg

20 – 40 mg/ml

1.8 – 60 mg/ml

2 – 60 mg

8 – 32 mg

25 – 200 mg/ml

0.1%

Cerenia® (maropitant citrate) injectable solution 10 mg/mL (NADA 141-263) is FDA-approved for the treatment of vomiting in dogs and cats. Cerenia® is also FDA-approved in tablet form (NADA 141-262) for the treatment of vomiting in dogs and may be used in an extralabel manner in cats. These formulations should be sufficient for urgent use. If longer term treatment is deemed necessary by the veterinarian, compounded formulations may be obtained pursuant to a patient-specific prescription.
Methocarbamol
(3/29/2023)
dog, cat

horse



dog, cat, horse
capsules

oral paste
oral powder
oral suspension

soft chew treat
flavored and quadrisected tablet
15 -250 mg

500 mg/mL
0.5 gm -12 gm/dose
30 – 300 mg/mL

50 -125 mg
500 mg
Methocarbamol in an oral suspension (30-300 mg/ml) for dogs and cats is on the List of Bulk Drug Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals. In addition, there are FDA-approved drugs that can be used as labeled, and FDAapproved methocarbamol products that can be used in an extralabel manner under 21 CFR Part 530 to treat the nominated conditions in dogs, cats, and horses in an urgent situation, until a patient-specific prescription can be filled, if needed.
Mirtazapine
(12/6/2023)
dog, cat soft chewable treats

oral suspension

oral paste

transdermal gel
1 – 3.75 mg

0.5 – 37.7 mg/ml

1.875 mg/ml

5 – 150 mg/ml
Mirtazapine BDS for compounding tablets (1 – 3.75 mg) and capsules (0.5 – 3.75 mg) is on the List of Bulk Drug Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals. FDA-approved tablets for humans (7.5/15/30/45 mg) can be used in an extralabel manner for dogs. Mirataz (mirtazapine transdermal ointment, 20 mg/g), NADA 141-481, is FDA-approved for use in cats and may be used in an extralabel manner in dogs, although FDA is not aware of evidence of adequate transdermal absorption of mirtazapine in dogs. These dosage forms may be administered to dogs and cats for urgent treatment until a patient-specific prescription for another dosage form can be filled.
Mitotane
(2/28/2023)
dog capsules

oral suspension

soft chew treat
any

any

any
Mitotane should not be needed for urgent treatment to avoid animal suffering or death. If a compounded mitotane product is deemed necessary by a veterinarian, a patient-specific prescription should suffice.
Neomycin sulfate/tetracaine HCl/triamcinolone acetonide
(4/20/2023)
dog, cat, horse otic ointment
topical ointment
topical powder
any
any
any
There are several FDA-approved and marketed drugs that can be used as labeled or in an extralabel manner for dogs, cats, and horses on an urgent basis. If a compounded preparation with neomycin, tetracaine HCl, and triamcinolone acetonide is needed, a patientspecific prescription should suffice.
Nitenpyram
(2/28/2023)
dog, cat oral solution

rectal gel
22.7 mg/mL

11.4 and 57 mg
FDA-approved Capstar (nitenpyram), NADA 141-175, can be used as labeled, or in an extralabel manner under 21 CFR Part 530, to treat the same conditions in dogs or cats in an urgent situation, until a patient-specific prescription can be filled, if needed.
Ondansetron
(2/8/2023)
dog, cat capsules 
oral solution soft chew treat transdermal gel
0.5 - 24 mg
0.7 - 40 mg/ml
2 mg
20 – 70 mg/ml
There are FDA-approved products that can be used as labeled, or in an extralabel manner under 21 CFR Part 530, to treat the nominated conditions in dogs and cats in an urgent situation, until a patient-specific prescription can be filled, if needed.
Pentosan polysulfate sodium
(12/20/2022)
dog, cat, horse capsules

oral suspension

injectable solution
10-800 mg

75-400 mg/ml

100-250 mg/ml
Zycosan (NADA 141-599) (pentosan polysulfate sodium 250 mg/ml) solution for injection is FDA-approved for use in horses for the control of clinical signs associated with osteoarthritis. There are numerous FDA-approved products that can be used as labeled or in an extralabel manner under 21 CFR part 530 in dogs, cats, and horses.
Pergolide mesylate
(4/21/2023)
horse capsule
oral granules 
oral suspension 
oral paste
oral powder packet
tablets, flavored
transdermal gel 
any There is a marketed FDA-approved animal drug containing the same active ingredient, in the same or similar dosage form, that can be used as labeled in horses, and the drug is not typically needed urgently. If the veterinarian determines a different drug formulation is needed, a patient-specific prescription can be filled.
Prazosin
(2/28/2023)
dog, cat soft chewable treat

transdermal gel

capsule
0.5 - 1 mg

2.5 - 10 mg/ml

1 - 20 mg
FDA-approved prazosin drug products for humans can be used in an extralabel manner under 21 CFR Part 530 in most dogs and cats. Prazosin is on the List of Bulk Drug Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals in several concentrations and dosage forms that can be used in small dogs and cats. The need for specialized drug formulations beyond these can be addressed using patient-specific prescriptions.
Pregabalin
(2/8/2023)
dog, cat capsules 10 - 55 mg There are FDA-approved products that can be used in an extralabel manner under 21 CFR Part 530 to treat the same conditions in dogs and cats in an urgent situation, until a patient-specific prescription can be filled, if needed.
Sucralfate
(2/28/2023)
dog, cat, horse


dog, horse

horse
capsules
oral paste
oral suspension

oral powder


oral powder (packet)
500 - 1,100 mg
250 - 500 mg/mL
2.5 - 500 mg/mL

250 mg/dose to 12 g/dose

10 g/packet
There are marketed FDA-approved human drugs containing sucralfate, in the same or similar dosage forms, that can be used in an extralabel manner under 21 CFR Part 530 to treat the same conditions in dogs, cats, and horses in an urgent situation. The FDA-approved human drugs can be used until a patient-specific prescription for a different dosage form is filled, if needed.
Telmisartan
(2/22/2023)
dog, cat capsules
oral suspension
soft chew treats
flavored tablets
0.5-47 mg
1-180 mg/mL
2-20 mg
10 mg
There are FDA-approved products that can be used as labeled, or in an extralabel manner under 21 CFR Part 530, to treat the same conditions in dogs and cats in an urgent situation, until a patient-specific prescription can be filled, if needed.
Toceranib phosphate
(2/8/2023)
dog, cat capsules
oral suspension 
soft chew treat 
2 - 180 mg
5 - 115 mg/ml
7 - 65 mg
Toceranib phosphate is FDA-approved for dogs (Palladia®, NADA 141-295) and can be used in an extralabel manner under 21 CFR Part 530 in cats. If a different dosage form is needed for longer term treatment of a specific patient, a patient-specific prescription can be filled.
Xylazine
(3/28/2023)
any any any FDA-approved xylazine products, can be used as labeled, or in an extralabel manner under 21 CFR Part 530, as a single agent or in combined drug protocols for sedation or immobilization of the nominated species.

NONFOOD-PRODUCING MINOR SPECIES

Bulk Drug Substance (BDS) Species Dosage form(s) Strength/concentration Reason
Amikacin
(2/8/2023)
birds, guinea pigs, chinchillas, hamsters, rats, mice, fish, and reptiles (including snakes, turtles, tortoises) injectable solution 200 mg/ml If an injectable solution is needed for urgent treatment, Amiglyde-V (NADA 127-892) or the amikacin injectable solutions FDA-approved for use in humans can be used in an extralabel manner under 21 CFR Part 530.
Azithromycin
(4/20/2023)
guinea pigs, birds (nonfood-producing), assorted captive exotic and zoo species

rabbits
any






any
any






any
Insufficient information was submitted to support the need for urgent use in these species.




Rabbits (except laboratory rabbits) are considered food-producing animals. Review of BDS nominations for food-producing animals is limited to antidotes for food-producing animals and sedatives and anesthetics for free-ranging wildlife.
Buprenorphine HCl
(4/24/2023)
large cats, bears, small exotic mammal pets, rodents (e.g., mice and rats), ferrets, large zoo animals

rabbits

injectable
polymeric matrix solution

injectable solution



oral solution
 

any
any

any



any
FDA-approved injectable solution is available as labeled for administration or for extralabel use under 21 CFR Part 530 for injection or oral administration. Specialty formulations can be obtained via patient-specific prescription and are not generally needed as office stock.

Rabbits (except laboratory rabbits) are considered food-producing animals. Review of BDS nominations for food-producing animals is limited to antidotes for food-producing animals and sedatives and anesthetics for free-ranging wildlife.
Butorphanol-Azaperone-Medetomidine (BAM)
(2/1/2022)
laboratory animals (mice, rats, and rabbits) fixed-combination injectable solution butorphanol (27.3 mg/ml)-azaperone (9.1 mg/ml)-medetomidine (10.9 mg/ml) Butorphanol and medetomidine are FDA-approved animal drugs available in concentrations that can be used in an extralabel manner under 21 CFR part 530 for sedation and anesthesia in laboratory animals. While FDA-approved azaperone is not marketed in the United States, azaperone tartrate is included on the List of Bulk Drug Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals and can be used to compound office stock for use in laboratory animals.
Chloramphenicol
(2/28/2023)
small mammal, birds oral capsule

oral suspension

otic ointment/solution/suspension
30 - 1000 mg

125 - 500 mg/mL

1 - 2%
Insufficient information was submitted to support the need for urgent use in birds and small mammals.
Corticotropin (ACTH)
(1/19/2023)
birds injectable 40 & 80 units/ml There are FDA-approved products that can be used in an extralabel manner under 21 CFR Part 530 in birds. There is lack of supporting information that this drug is needed on an urgent basis in these species.
Haloperidol
(2/1/2022)
large herbivores (zoo hoofed stock), exotic pet birds Injectable (lactate, aqueous)

capsules

oral solution

oral suspension
20 mg/ml



60 mg

0.1 mg/ml to 2 mg/ml

2 mg/ml
Haloperidol is available as FDA-approved human drug products that can be used as formulated or used to compound a different concentration or to add flavor if needed.
Naloxone hydrochloride
(2/1/2022)
bears, birds, camelids, canids, pocket pets, cervids, otters, primates, rabbits, lab rodents, ratites, sheep, and free-ranging wild animals injectable solution 1 mg/ml There are FDA-approved naloxone 1 mg/ml injection products that can be used in animals in an extralabel manner under 21 CFR part 530.
Xylazine
(3/28/2023)
any any any FDA-approved xylazine products, can be used as labeled, or in an extralabel manner under 21 CFR Part 530, as a single agent or in combined drug protocols for sedation or immobilization of the nominated species.

FOOD-PRODUCING ANIMALS OR FREE-RANGING WILDLIFE SPECIES

Bulk Drug Substance (BDS) Species Dosage form(s) Strength/concentration Reason
Azithromycin
(4/20/2023)
rabbits any any Azithromycin is not an antidote, sedative, or anesthetic.
Buprenorphine
HCl (4/24/2023)
rabbits, free-ranging wildlife any any Buprenorphine is not an antidote, sedative, or anesthetic.
Naloxone hydrochloride
(2/1/2022)
sheep and free-ranging wild animals injectable solution 1 mg/ml There are FDA-approved naloxone 1 mg/ml injection products that can be used in animals in an extralabel manner under 21 CFR part 530.
Xylazine
(3/28/2023)
any any any FDA-approved xylazine products, can be used as labeled, or in an extralabel manner under 21 CFR Part 530, as a single agent or in combined drug protocols for sedation or immobilization of the nominated species.

These bulk drug substances are not covered by FDA’s enforcement discretion policy described in GFI #256. FDA will consider them for inclusion on any List if they are nominated again with new information, using the nomination procedure described in the appendix to GFI #256.

FDA will accept nominations of additional bulk drug substances at any time and will continue to review nominations and update lists. For information on how to submit a bulk drug substance nomination, see the appendix to Guidance for Industry #256 Compounding Animal Drugs from Bulk Drug Substances.

To view information that was previously submitted for these nominations, click on the hyperlinked Docket ID for each of these nominations, below.

Docket ID: FDA-2015-N-1196-0005
Substance(s): Prednisolone and prednisone 2.5mg, 5mg, 10mg, 20mg, 50mg, doxycycline 50mg, 100mg, 200mg, ketoconazole 200mg, cyclosporin 2% ophthalmic suspension

Docket ID: FDA-2015-N-1196-0006
Substance(s): Lanolin, enrofloxacin, triamcinolone, and neomycin in combination

Docket ID: FDA-2015-N-1196-0007
Substance(s): Doxycycline, metronidazole, methimazole, ponazuril

Docket ID: FDA-2015-N-1196-0009
Substance(s): List of 85 bulk drug substances

Docket ID: FDA-2015-N-1196-0017
Substance(s): Copper peptide, Superoxide dismutase

Docket ID: FDA-2015-N-1196-0018
Substance(s): Ophthalmic: idoxuridine, cidofivir, cyclosporine 2%, tacrolimus 2%, fluconazole, voriconazole

Docket ID: FDA-2015-N-1196-0019
Substance(s): List of 23 bulk drug substances

Docket ID: FDA-2015-N-1196-0020
Substance(s): Methimazole, amlodipine, ondansetron, prednisolone, prednisone, metronidazole, griseofulvin, cyproheptadine, mirtazapine, doxycycline

Docket ID: FDA-2015-N-1196-0021
Substance(s): Apomorphine, methocarbamol, buprenorphine, antibiotics, fentanyl, morphine

Docket ID: FDA-2015-N-1196-0024
Substance(s): Metronidazole, baytril, buprenorphine, morphine, prazosin, prednisone, methocarbamol, omeprazole

Docket ID: FDA-2015-N-1196-0036
Substance(s): Tylan soluble powder

Docket ID: FDA-2015-D-1176-0113
Substance(s): Diclofenac

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