Alprazolam
- Product NDC
- 64980-396
- 11-digit product format
- 649800396
- Labeler code
- 64980
- Product ID
- 64980-396_f69a9cd9-e516-4a6a-adba-29db5cee019c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc.
- Application
- ANDA203346
- Marketing category
- ANDA
- Marketing start
- 2017-11-07
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 64980-396-01 | 64980039601 | 100 TABLET in 1 BOTTLE (64980-396-01) | 100 tablet | 2017-11-07 | 0000-00-00 | No | No | Current |
| 64980-396-10 | 64980039610 | 1000 TABLET in 1 BOTTLE (64980-396-10) | 1000 tablet | 2017-11-07 | 0000-00-00 | No | No | Current |
| 64980-396-50 | 64980039650 | 500 TABLET in 1 BOTTLE (64980-396-50) | 500 tablet | 2017-11-07 | 0000-00-00 | No | No | Current |