Due for re-check: the scheduled review date of 2026-09-04 has passed. Every value below still carries the source it was taken from and the passage that states it — check it against the link.
76045-121-11 · Hydromorphone Hydrochloride Injection · Fresenius Kabi USA, LLC
What is the package ndc for 76045-121-11 · Hydromorphone Hydrochloride Injection · Fresenius Kabi USA, LLC?
For 76045-121-11 · Hydromorphone Hydrochloride Injection · Fresenius Kabi USA, LLC, package ndc is 76045-121-11; generic name is Hydromorphone Hydrochloride Injection; manufacturer is Fresenius Kabi USA, LLC; status is Current; availability now is Available, recorded from its source on 2026-09-01.
"initial_posting_date": "11/01/2017", "package_ndc": "76045-121-11", "generic_name": "Hydromorphone Hydrochloride Injection", "contact_info": "888-386-1300", "availability": "Available", "related_info": "Check wholesalers for inventory"
— api.fda.gov, retrieved 2026-09-01
- Package NDC
- 76045-121-11 verified
- Generic name
- Hydromorphone Hydrochloride Injection verified
- Manufacturer
- Fresenius Kabi USA, LLC verified
- Status
- Current verified
- Availability now
- Available verified
- FDA note
- Check wholesalers for inventory verified
- Initial posting date
- 11/01/2017 verified
- Last update date
- 08/25/2026 verified
- Days in shortage
- 3226 our reading
- Dosage form
- Injection verified
- Therapeutic category
- Analgesia/Addiction verified
- Reason for shortage
- Other also on this page
Values marked our reading are our classification of what the source says — the source does not print them in those words. The quote below is the evidence for each one; judge it yourself.
Where each value comes from
The values above are stated away from the sentence quoted with the answer, so the passage that states them is shown here too.
Manufacturer, Status, Last update date, Dosage form and Therapeutic category
"update_date": "08/25/2026", "therapeutic_category": [ "Analgesia/Addiction" ], "dosage_form": "Injection", "presentation": "Dilaudid, Injection, .2 mg/1 mL (NDC 76045-121-11)", "company_name": "Fresenius Kabi USA, LLC", "status": "Current"
— all from api.fda.gov, retrieved 2026-09-01
The same source also states
"initial_posting_date": "11/01/2017", "package_ndc": "76045-121-11", "generic_name": "Hydromorphone Hydrochloride Injection", "contact_info": "888-386-1300", "availability": "Unavailable", "related_info": "Estimated recovery: TBD; Check wholesalers for inventory."
— api.fda.gov, retrieved 2026-09-03
Source
- api.fda.govhttps://api.fda.gov/drug/shortages.json?search=company_name%3A%22Fresenius%20Kabi%20USA,%20LLC%22+AND+generic_name%3A%22Hydromorphone%20Hydrochloride%20Injection%22+AND+status%3A%22Current%22&limit=1000