Hydromorphone Hydrochloride Injection
Fresenius Kabi USA, LLC · Available
Open FDA's page for this record- Update type
- Reverified
- Initial posting date
- 10/31/2017
- Package NDC
- 63323-851-10
- Generic name
- Hydromorphone Hydrochloride Injection
- Contact info
- 888-386-1300
- Availability
- Available
- Related info
- Check wholesalers for inventory
- Update date
- 11/03/2026
- Dosage form
- Injection
- Presentation
- Hydromorphone Hydrochloride, Injection, 10 mg/1 mL (NDC 63323-851-10)
- Company name
- Fresenius Kabi USA, LLC
- Status
- Current
- Therapeutic category
- Analgesia/Addiction
- Harmonized identifiers (openFDA)
- Application number
- NDA019034
- Brand name
- HYDROMORPHONE HYDROCHLORIDE
- Generic name
- HYDROMORPHONE HYDROCHLORIDE
- Manufacturer name
- Fresenius Kabi USA, LLC
- Product NDC
- 63323-851, 63323-852, 63323-853, 63323-854
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
- Substance name
- HYDROMORPHONE HYDROCHLORIDE
- RxCUI
- 897653, 897753, 1724276, 1724338, 1724340, 1724341
- SPL ID
- 2cfa0a3e-eb57-4dea-ae2c-0b91176f0f67
- SPL set ID
- e034eb96-03e0-46e1-8b92-5e1f94555e7b
- Package NDC
- 63323-851-03, 63323-851-10, 63323-851-07, 63323-851-15, 63323-851-50, 63323-852-03, 63323-852-25, 63323-853-03, 63323-853-25, 63323-854-03, 63323-854-10
- UNII
- L960UP2KRW