Alprazolam
- Product NDC
- 68071-5113
- 11-digit product format
- 680715113
- Labeler code
- 68071
- Product ID
- 68071-5113_f19f4f0d-3d62-ebfe-e053-2a95a90af6ea
- 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
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 68071-5113-3 | 68071511303 | 30 TABLET in 1 BOTTLE (68071-5113-3) | 30 tablet | 2019-11-18 | 0000-00-00 | No | No | Current |
| 68071-5113-5 | 68071511305 | 15 TABLET in 1 BOTTLE (68071-5113-5) | 15 tablet | 2019-11-18 | 0000-00-00 | No | No | Current |