Alprazolam
- Product NDC
- 43063-367
- 11-digit product format
- 430630367
- Labeler code
- 43063
- Product ID
- 43063-367_adc8bfb4-466b-0ad9-e053-2995a90a4727
- 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 |
|---|---|---|---|---|---|
| 43063-367-06 | EA - Each | 43063-367 | 6551a4e5-e3b1-44ce-8834-dab08c474de3 | 1 | 2014-05-02 |
| 43063-367-15 | EA - Each | 43063-367 | a5a49971-4a51-4f7e-8e8c-038c1624a0a6 | 1 | 2012-07-24 |
| 43063-367-30 | EA - Each | 43063-367 | 4cbb534e-eb93-462f-b880-ba61e9d909f7 | 1 | 2012-07-24 |
| 43063-367-60 | EA - Each | 43063-367 | 0a9954f4-3546-481f-8f86-063822d477f9 | 1 | 2012-07-24 |
| 43063-367-90 | EA - Each | 43063-367 | 05484734-0458-4dbc-a151-100c9bf25277 | 1 | 2012-07-24 |
| 43063-367-98 | EA - Each | 43063-367 | af111fa5-83bb-4aaf-b562-5bfa828ab656 | 1 | 2012-07-24 |