Morphine Sulfate Injection
Hospira, Inc., a Pfizer Company · Available
Open FDA's page for this record- Update type
- Reverified
- Initial posting date
- 10/31/2017
- Package NDC
- 0409-3815-12
- Generic name
- Morphine Sulfate Injection
- Contact info
- 844-646-4398
- Availability
- Available
- Update date
- 09/22/2026
- Dosage form
- Injection
- Presentation
- Morphine Sulfate, Injection, 10 mg/10 mL (1 mg/mL) (NDC 0409-3815-12)
- Company name
- Hospira, Inc., a Pfizer Company
- Status
- Current
- Therapeutic category
- Analgesia/Addiction
- Harmonized identifiers (openFDA)
- Application number
- ANDA073510
- Brand name
- MORPHINE SULFATE
- Generic name
- MORPHINE SULFATE
- Manufacturer name
- Hospira, Inc.
- Product NDC
- 0409-3815, 0409-3814
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- EPIDURAL, INTRATHECAL, INTRAVENOUS
- Substance name
- MORPHINE SULFATE
- RxCUI
- 1728783, 1728800
- SPL ID
- 0a2ba20b-448f-4412-9899-b82040ebfa7d
- SPL set ID
- 1d181906-f3ec-4222-1883-e61577a3122e
- Package NDC
- 0409-3814-11, 0409-3814-12, 0409-3815-11, 0409-3815-12
- UNII
- X3P646A2J0
