CBER-Regulated Products: Current Shortages
The following table identifies current shortages of CBER-regulated products. The information contained in this table is generally provided to CBER by the manufacturer of the CBER-regulated product that is in shortage. CBER is committed to ensuring that the information in the table is current, and works closely with the manufacturer to obtain accurate information.
Please refer to the Resources for You box at the bottom of the page for a complete listing of all CBER approved, licensed, and cleared products, as well as CDC's recommended immunization schedules for adult and children.
Additional information regarding possible causes for CBER-regulated product shortages is provided on
CBER-Regulated Products: Possible Causes of Shortages Page.
Product | Manufacturer and Manufacturer Contact Information | Product Availability and Estimated Shortage Duration (when known) | Shortage Reason (per FDASIA)* | Additional Information | Date |
---|---|---|---|---|---|
Albumin (Human)-kjda ALBUMINEX 5%® 12.5g in 250mL NDC Number: 64208-2510-2 25g in 500mL NDC Number: 64208-2510-6 |
Bio Products Laboratory For questions, please call customer service at: 1-844-4BPLUSA (1-844-427-5872) |
ALBUMINEX 5%® Albumin (Human)-kjda is currently available in limited supply. | Demand increase in the drug or biological product | Bio Products Laboratory (BPL) anticipates that due to high demand and manufacturing schedule ALBUMINEX 5%® Albumin (Human)-kjda 250ml and 500ml vials will go on backorder between late October 2022 and mid-November 2022. BPL anticipates additional release and availability of ALBUMINEX 5%® 250mL and 500mL vials in the December 2022/January 2023 timeframe. There continues to be ample supply of ALBUMINEX 25%® available through the exclusive distributor of ALBUMINEX®, FFF Enterprises, Inc. To check availability and to order ALBUMINEX®, please contact FFF Enterprises directly at: 1-800-843-7477 or: Albumin (fffenterprises.com) |
Onset: November 2022 Ongoing |
BCG Live (Intravesical) TICE® BCG NDC Number: 00052-0602-02 50 mg lyophilized powder |
Organon Teknika, Corporation LLC, a subsidiary of Merck & Co, Inc. For questions, please call customer service at: 1-800-NSC-MERCK 1-800-672-6372 |
TICE® BCG, BCG Live (Intravesical) is currently available. In order to help manage inventory and to minimize disruption to patient care when demand exceeds production plans and available inventory product will be placed on allocation. |
Demand increase in the drug or biological product | Because of increased global demand and as the only source of BCG Live (Intravesical) in the United States and many other countries, Merck anticipates supply constraints for TICE® BCG for the foreseeable future. To minimize disruption to patient care and address the current imbalance between supply and increased global demand TICE® BCG will be under allocation when demand exceeds production plans and available inventory. Please Note: In the past, Merck has provided preservative-free saline with certain orders of TICE® BCG. Merck is no longer able to provide saline with TICE® BCG and has discontinued the distribution of saline with TICE® BCG. For questions, please call Merck customer service at: 1-800-NSC-MERCK 1-800-672-6372 Or visit http://www.merck.com/product/oncology/home.html |
Onset: January 2019 Updated: July 2020 Ongoing |
Venoms, Honey Bee Venom Venoms, Mixed Vespid Venom Protein Venoms, Wasp Venom Protein Venoms, White Faced Hornet Venom Protein Venoms, Yellow Hornet Venom Protein Venoms, Yellow Jacket Venom Protein Pharmalgen® Venoms, Honey Bee Venom NDC Number: 52709-0801-1 1.2 mL in 1 VIAL, SINGLE-DOSE Venoms, Mixed Vespid Venom Protein NDC Number: 52709-1201-1 1.2 mL in 1 VIAL, SINGLE-DOSE Venoms, Wasp Venom Protein NDC Number: 52709-1301-1 1.2 mL in 1 VIAL, SINGLE-DOSE Venoms, White Faced Hornet Venom Protein NDC Number: 52709-1101-1 1.2 mL in 1 VIAL, SINGLE-DOSE Venoms, Yellow Hornet Venom Protein NDC Number: 52709-1001-1 1.2 mL in 1 VIAL, SINGLE-DOSE Venoms, Yellow Jacket Venom Protein NDC Number: 52709-0901-1 1.2 mL in 1 VIAL, SINGLE-DOSE |
ALK - Abello A/S Customer Service: 1-512-251-0037 For questions concerning patient treatment options or manufacturer conversions, please contact ALK Scientific Services: 1-800-325-7354 |
At this time Pharmalgen® (lyophilized allergenic venom extract) products are unavailable. | Other | For general questions and questions concerning supply, please contact ALK Customer Service at: 1-512-251-0037 For questions concerning patient treatment options or manufacturer conversions, please contact ALK Scientific Services at: 1-800-325-7354 |
Onset: November 2016 Updated: November 2019 Ongoing |
BCG Vaccine NDC Number: 00052-0603-02 50 mg lyophilized powder |
Organon Teknika, Corporation LLC, a subsidiary of Merck & Co, Inc. For questions, please call Merck customer service at: 1-800-NSC-MERCK (1-800-672-6372 |
BCG Vaccine, for tuberculosis prevention is currently unavailable. | Other | Merck is developing a control mechanism to ensure that customer orders being placed for BCG Vaccine, are for tuberculosis prevention. BCG vaccine will remain unavailable until a new ordering process is implemented. For questions, please call Merck customer service at: 1-800-NSC-MERCK (1-800-672-6372) Or visit https://www.merckorders.com |
Onset: July 2019 Updated: November 2019 Ongoing |
Immune Globulin Intravenous (Human) Gammaplex® NDC Number: 64208-8234 Gammaplex 5% Liquid NDC Number: 64208-8235 Gammaplex 10% Liquid |
Bio Products Laboratory For questions, please call BPL customer service at: 1-844-4BPLUSA (1-844-427-5872) |
Gammaplex® Immune Globulin Intravenous (Human) is currently available but due to continued high demand and manufacturing schedule, there is a limited supply of this product, which is presently being allocated to a limited number of customers. | Other | For questions, please call BPL customer service at: 1-844-4BPLUSA (1-844-427-5872) |
Onset: October 2018 Updated: August 2019 Ongoing |
* FDASIA added several new, drug-shortage related sections to the FD&C Act, including section 506E. Section 506E of the FD&C Act further requires FDA to include on the shortages list the reason for the shortage, choosing from the following categories:
- Requirements relating to complying with current good manufacturing practices (CGMP);
- Regulatory delay;
- Shortage of an active ingredient;
- Shortage of an inactive ingredient component;
- Discontinuation of the manufacture of the drug or biological product;
- Delay in shipping of the drug or biological product;
- Demand increase in the drug or biological product; or
- Other.
Resources for You
- Complete List of Licensed Products and Establishments
- Vaccines Licensed for Use in the United States
- Complete List of Currently Approved NDA and ANDA Application Submissions
- Complete List of Currently Approved Premarket Approvals (PMAs)
- Complete List of Substantially Equivalent 510(k) Device Applications
- CDC's Recommended Immunization Schedules for Adults and Children
- Office of Compliance and Biologics Quality (OCBQ)