Alprazolam
- Product NDC
- 71335-0215
- 11-digit product format
- 713350215
- Labeler code
- 71335
- Product ID
- 71335-0215_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 |
|---|---|---|---|---|---|
| 71335-0215-0 | EA - Each | 71335-0215 | 89894232-2bfe-4c8e-897e-2e1089dee873 | 1 | 2018-01-12 |
| 71335-0215-1 | EA - Each | 71335-0215 | 80b33ee1-8232-403d-9dbc-1bf28edc9eb2 | 1 | 2018-01-12 |
| 71335-0215-2 | EA - Each | 71335-0215 | 12fc4891-0709-4feb-90f4-bbde50b9082e | 1 | 2018-01-12 |
| 71335-0215-3 | EA - Each | 71335-0215 | 8eb7122b-a918-46b1-b684-344d45825199 | 1 | 2018-01-12 |
| 71335-0215-4 | EA - Each | 71335-0215 | adfd53b8-cd2b-4950-a42e-0d5bc8b5af53 | 1 | 2018-01-12 |
| 71335-0215-5 | EA - Each | 71335-0215 | d8bee7d5-3d44-4769-a7cc-87112a9c762f | 1 | 2018-01-12 |
| 71335-0215-6 | EA - Each | 71335-0215 | 466ba927-a008-4628-bb90-7c9e74f75783 | 1 | 2018-01-12 |
| 71335-0215-7 | EA - Each | 71335-0215 | 27c5012d-bb6f-4b4b-afee-f3e22cb3852a | 1 | 2018-01-12 |
| 71335-0215-8 | EA - Each | 71335-0215 | 4683c225-9aee-41b6-ac58-54940982ab42 | 1 | 2018-01-12 |
| 71335-0215-9 | EA - Each | 71335-0215 | 8c5081b0-f5b6-4970-88a5-51372c4fdf14 | 1 | 2018-01-12 |