Morphine sulfate
- Product NDC
- 72162-1792
- 11-digit product format
- 721621792
- Labeler code
- 72162
- Product ID
- 72162-1792_9a1ca529-8268-4be3-b03f-b2f2238cc9dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- morphine sulfate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078761
- Marketing category
- ANDA
- Marketing start
- 2012-05-11
- Substance
- MORPHINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| X3P646A2J0 | MORPHINE SULFATE | 6211-15-0 | MORPHINE SULFATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1792-1 | 72162179201 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1792-1) | 2012-05-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Morphine sulfate | Bryant Ranch Prepack | 2024-04-04 | HUMAN PRESCRIPTION DRUG LABEL | 101 |