Alprazolam
- Product NDC
- 83008-010
- 11-digit product format
- 830080010
- Labeler code
- 83008
- Product ID
- 83008-010_deea44c9-45a0-4cb1-afc9-770d02e55697
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 2023-03-07
- Marketing end
- 2026-08-31
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| YU55MQ3IZY | ALPRAZOLAM | 28981-97-7 | ALPRAZOLAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 83008-010-30 | 83008001030 | 30 TABLET in 1 BOTTLE (83008-010-30) | 30 tablet | 2023-03-07 | 2026-08-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | Quality Care Products, LLC | 2024-12-19 | HUMAN PRESCRIPTION DRUG LABEL | 4 |