Morphine Sulfate
- Product NDC
- 17856-0406
- 11-digit product format
- 178560406
- Labeler code
- 17856
- Product ID
- 17856-0406_e0729d8c-f965-4436-9ea3-a54d7b86811f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Morphine Sulfate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- NDA022195
- Marketing category
- NDA
- Marketing start
- 2008-03-17
- Marketing end
- 0000-00-00
- Substance
- MORPHINE SULFATE
- Active strength
- 100 mg/5mL
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record