Alprazolam
- Product NDC
- 43063-364
- 11-digit product format
- 430630364
- Labeler code
- 43063
- Product ID
- 43063-364_adc8aa62-7cbb-4886-e053-2a95a90a7f79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA074174
- Marketing category
- ANDA
- Marketing start
- 2007-03-28
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 43063-364-06 | EA - Each | 43063-364 | 4a654fa5-a717-478b-a45d-efb8ab0132bf | 1 | 2012-07-24 |
| 43063-364-30 | EA - Each | 43063-364 | a181397a-82eb-40f9-8a6c-79e3d9bb7a8c | 1 | 2012-07-24 |
| 43063-364-40 | EA - Each | 43063-364 | f0642cd8-8db0-415a-b6c3-20ebb5e5d67c | 1 | 2012-07-24 |
| 43063-364-60 | EA - Each | 43063-364 | 51e59f68-80c7-4c03-be17-eebc909e0346 | 1 | 2012-07-24 |
| 43063-364-90 | EA - Each | 43063-364 | 968f31d6-5708-450d-a68b-3db7b3f4275c | 1 | 2012-07-24 |
| 43063-364-98 | EA - Each | 43063-364 | 54bef469-3218-4d49-8bd5-0d95dc2fe1a3 | 1 | 2012-07-24 |