MORPHINE SULFATE
- Product NDC
- 61919-413
- 11-digit product format
- 619190413
- Labeler code
- 61919
- Product ID
- 61919-413_83d6a4c3-d085-3ac9-e053-2a91aa0aa09f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MORPHINE SULFATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECTRX
- Application
- NDA022207
- Marketing category
- NDA
- Marketing start
- 2019-03-04
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-413-30 | 61919041330 | 30 TABLET in 1 BOTTLE (61919-413-30) | 30 tablet | 2019-03-04 | 0000-00-00 | No | No | Current |