Morphine Sulfate
- Product NDC
- 0409-2028
- 11-digit product format
- 004092028
- Labeler code
- 0409
- Product ID
- 0409-2028_ee99d46c-362a-44d7-9ea3-6bfdb1068845
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MORPHINE SULFATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA019917
- Marketing category
- NDA
- Marketing start
- 2006-11-28
- Marketing end
- 0000-00-00
- Substance
- MORPHINE SULFATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record