Morphine sulfate
- Product NDC
- 55700-367
- 11-digit product format
- 557000367
- Labeler code
- 55700
- Product ID
- 55700-367_f946952f-d683-4bd8-a173-371ec414e5ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Morphine sulfate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA203849
- Marketing category
- ANDA
- Marketing start
- 2015-10-26
- Marketing end
- 0000-00-00
- Substance
- MORPHINE SULFATE
- Active strength
- 30 mg/1
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| X3P646A2J0 | MORPHINE SULFATE | 6211-15-0 | MORPHINE SULFATE |