Morphine Sulfate
- Product NDC
- 62559-171
- 11-digit product format
- 625590171
- Labeler code
- 62559
- Product ID
- 62559-171_16a27365-2e64-4e8f-b46a-3cc41906872d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Morphine Sulfate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA205509
- Marketing category
- ANDA
- Marketing start
- 2018-07-09
- Marketing end
- 2022-07-31
- Substance
- MORPHINE SULFATE
- Active strength
- 20 mg/5mL
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 62559-171-01 | 62559017101 | 100 mL in 1 BOTTLE (62559-171-01) | 100 ml | 2018-07-09 | 2021-08-31 | No | No | Current |
| 62559-171-05 | 62559017105 | 500 mL in 1 BOTTLE (62559-171-05) | 500 ml | 2018-07-09 | 2022-02-28 | No | No | Current |