Morphine Sulfate
- Product NDC
- 17856-0403
- 11-digit product format
- 178560403
- Labeler code
- 17856
- Product ID
- 17856-0403_92743a73-e7c8-432e-ad30-c8c5bfc412b5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Morphine Sulfate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- NDA022195
- Marketing category
- NDA
- Marketing start
- 2018-11-21
- 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