Alprazolam
- Product NDC
- 68071-4831
- 11-digit product format
- 680714831
- Labeler code
- 68071
- Product ID
- 68071-4831_de47eb48-1b44-7dc1-e053-2995a90a9e72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2018-07-09
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 2 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4831-9 | 68071483109 | 90 TABLET in 1 BOTTLE (68071-4831-9) | 90 tablet | 2019-04-03 | 0000-00-00 | No | No | Current |