Alprazolam
- Product NDC
- 63629-2942
- 11-digit product format
- 636292942
- Labeler code
- 63629
- Product ID
- 63629-2942_c89986aa-e7a2-46ed-9df5-784a1bd7e09d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 2008-04-02
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-2942-0 | EA - Each | 63629-2942 | c507aabd-4601-47ae-bda8-ab8c8c0e528a | 1 | 2012-07-24 |
| 63629-2942-1 | EA - Each | 63629-2942 | ce7fb088-23f2-49da-88a6-e689a86c07d1 | 1 | 2012-07-24 |
| 63629-2942-2 | EA - Each | 63629-2942 | 1fb66113-4b9b-40a4-8346-c505c6fb246c | 1 | 2012-07-24 |
| 63629-2942-3 | EA - Each | 63629-2942 | 770f51ff-9d8a-47f9-8640-69837d328d45 | 1 | 2012-07-24 |
| 63629-2942-4 | EA - Each | 63629-2942 | cfc610ed-f89a-4811-8e9a-2ffd1b16a473 | 1 | 2012-07-24 |
| 63629-2942-5 | EA - Each | 63629-2942 | d5581c5d-ec33-49d8-beb9-1d754b940698 | 1 | 2012-07-24 |
| 63629-2942-6 | EA - Each | 63629-2942 | 248ff782-4035-49b8-8b6d-8338fe85e701 | 1 | 2012-07-24 |
| 63629-2942-7 | EA - Each | 63629-2942 | d73d5a1c-2651-4fcb-a198-83d7d8884537 | 1 | 2012-07-24 |
| 63629-2942-8 | EA - Each | 63629-2942 | 9283135e-d7d1-4775-9de6-decff83f43a5 | 1 | 2012-07-24 |
| 63629-2942-9 | EA - Each | 63629-2942 | 81207e19-8aeb-494b-ba58-7ab8c899446b | 1 | 2012-07-24 |