Alprazolam
- Product NDC
- 68071-2794
- 11-digit product format
- 680712794
- Labeler code
- 68071
- Product ID
- 68071-2794_e4164d25-9eb4-72a8-e053-2a95a90a5d85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 1993-10-01
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 68071-2794-6 | 68071279406 | 6 TABLET in 1 BOTTLE (68071-2794-6) | 6 tablet | 2022-07-18 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | NuCare Pharmaceuticals,Inc. | 2022-07-18 | HUMAN PRESCRIPTION DRUG LABEL | 1 |