Drug shortages

Hydromorphone Hydrochloride Injection

Hospira, Inc., a Pfizer Company · Limited Availability · Reason: Other

Current0409-4264-01Analgesia/Addiction
Open FDA's page for this record
Update type
Revised
Initial posting date
11/01/2017
Package NDC
0409-4264-01
Generic name
Hydromorphone Hydrochloride Injection
Contact info
844-646-4398
Availability
Limited Availability
Related info
Limited Supply Available. Next Delivery: September 2026; Estimated Recovery: December 2026; Shortage per Manufacturer: Manufacturing Delay
Update date
09/22/2026
Dosage form
Injection
Presentation
Hydromorphone Hydrochloride, Injection, 0.5 mg/0.5 mL NexJect™ Single-dose Syringe Luer Lock (no needle) (NDC 0409-4264-01)
Company name
Hospira, Inc., a Pfizer Company
Shortage reason
Other
Status
Current
Therapeutic category
Analgesia/Addiction
Harmonized identifiers (openFDA)
Application number
NDA200403
Brand name
HYDROMORPHONE HYDROCHLORIDE
Generic name
HYDROMORPHONE HYDROCHLORIDE
Manufacturer name
Hospira, Inc.
Product NDC
0409-4264, 0409-1283, 0409-1312, 0409-1805
Product type
HUMAN PRESCRIPTION DRUG
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Substance name
HYDROMORPHONE HYDROCHLORIDE
RxCUI
897756, 897757, 1433251, 1724383, 1724644, 2675350
SPL ID
766e302a-2d03-4d93-b237-2348b57ee517
SPL set ID
f9ca2ef5-46d8-475a-a26e-f7c8becd6db7
Package NDC
0409-1283-17, 0409-1283-37, 0409-1312-16, 0409-1312-36, 0409-4264-11, 0409-4264-01, 0409-1805-10, 0409-1805-01
UNII
L960UP2KRW
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.