Alprazolam
- Product NDC
- 43063-370
- 11-digit product format
- 430630370
- Labeler code
- 43063
- Product ID
- 43063-370_b4dd15f3-caa5-4f86-e053-2995a90abf5a
- 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
- 0 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 |
|---|---|---|---|---|---|
| 43063-370-05 | EA - Each | 43063-370 | cad70f16-1868-457a-913b-792b140e3868 | 1 | 2013-02-13 |
| 43063-370-20 | EA - Each | 43063-370 | f06eca19-f7f6-464b-b961-5b9807d6d478 | 1 | 2013-02-13 |
| 43063-370-30 | EA - Each | 43063-370 | 0fe35df4-44a3-4684-8203-da0d5509c1f8 | 1 | 2016-11-08 |
| 43063-370-60 | EA - Each | 43063-370 | 5fd5d305-b507-403c-b9f6-77b73ec61928 | 1 | 2013-02-13 |
| 43063-370-90 | EA - Each | 43063-370 | 6f995514-4912-4504-9b92-b80211f7590d | 1 | 2013-02-13 |
| 43063-370-98 | EA - Each | 43063-370 | feaa5706-64e3-4d1f-9d51-a4eaa895d8ad | 1 | 2013-02-13 |