Alprazolam
- Product NDC
- 71335-0247
- 11-digit product format
- 713350247
- Labeler code
- 71335
- Product ID
- 71335-0247_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
- 1 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 |
|---|---|---|---|---|---|
| 71335-0247-0 | EA - Each | 71335-0247 | 27c74c5e-00a6-40a2-9513-733bf966b861 | 1 | 2018-01-12 |
| 71335-0247-1 | EA - Each | 71335-0247 | 852c5a0a-87d4-4e4f-a5fa-78ac42d0a71c | 1 | 2018-01-12 |
| 71335-0247-2 | EA - Each | 71335-0247 | dc8ad3ac-6d4d-49c2-9ba1-ed5124a715c6 | 1 | 2018-01-12 |
| 71335-0247-3 | EA - Each | 71335-0247 | 12d01bfa-ade1-4f1e-a79f-706db9890761 | 1 | 2018-01-12 |
| 71335-0247-4 | EA - Each | 71335-0247 | f35d57f3-da97-4d7a-89ee-751711ee4555 | 1 | 2018-01-12 |
| 71335-0247-5 | EA - Each | 71335-0247 | d9ca1ad4-dfd8-4f50-8083-fb0cf07d0474 | 1 | 2018-01-12 |
| 71335-0247-6 | EA - Each | 71335-0247 | d20be9f1-6c9e-415a-bacf-cf37b9166cf8 | 1 | 2018-01-12 |
| 71335-0247-7 | EA - Each | 71335-0247 | 55d5cf01-b459-41d6-b333-1e4d68364b07 | 1 | 2018-01-12 |
| 71335-0247-8 | EA - Each | 71335-0247 | 40cce949-326f-4de6-9d95-8bd788fd9ea3 | 1 | 2018-01-12 |
| 71335-0247-9 | EA - Each | 71335-0247 | 8d6d183a-37db-4efa-a8e3-a0e4e053ba06 | 1 | 2018-01-12 |