Alprazolam
- Product NDC
- 71335-0163
- 11-digit product format
- 713350163
- Labeler code
- 71335
- Product ID
- 71335-0163_14d82b8a-1bb2-4550-9c25-1a82a2f108a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200739
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-0163-1 | EA - Each | 71335-0163 | 7516f2bf-f39d-47e6-82b3-bd9168c7e354 | 1 | 2018-03-08 |
| 71335-0163-2 | EA - Each | 71335-0163 | 6d11b627-691c-4898-af93-cdcc7f885014 | 1 | 2018-03-08 |
| 71335-0163-3 | EA - Each | 71335-0163 | 599d3108-8fc9-4d79-90c1-8c5c9e4efb3f | 1 | 2018-03-08 |
| 71335-0163-4 | EA - Each | 71335-0163 | 51583bc8-826f-4a2c-baf8-41b6a8c56717 | 1 | 2018-03-08 |
| 71335-0163-5 | EA - Each | 71335-0163 | d4ffbd2f-eb90-4b1e-801e-db8b2a3e32f6 | 1 | 2018-03-08 |
| 71335-0163-6 | EA - Each | 71335-0163 | 835b31e6-8080-45d0-a8b3-010f15a2c6e6 | 1 | 2018-03-08 |
| 71335-0163-7 | EA - Each | 71335-0163 | b8b3909d-c8a2-4080-87fc-f8be82c04c75 | 1 | 2018-03-08 |
| 71335-0163-8 | EA - Each | 71335-0163 | b00884f5-8844-4cc1-af3a-da4de7bf5f7b | 1 | 2018-03-08 |
| 71335-0163-9 | EA - Each | 71335-0163 | 1534a69b-8535-4066-91a1-cb16597d6948 | 1 | 2018-03-08 |