Alprazolam
- Product NDC
- 63187-916
- 11-digit product format
- 631870916
- Labeler code
- 63187
- Product ID
- 63187-916_513bc814-d2ed-4444-89f3-e18f907e0952
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA074112
- Marketing category
- ANDA
- Marketing start
- 1995-12-29
- Substance
- ALPRAZOLAM
- Active strength
- .25 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 | Sample | Exclude flag | Status |
|---|
| 63187-916-30 | 63187091630 | 60 TABLET in 1 BOTTLE (63187-916-30) | 60 tablet | 2017-09-01 | No | No | Historical |
| 63187-916-60 | 63187091660 | 60 TABLET in 1 BOTTLE (63187-916-60) | 60 tablet | 2017-09-01 | No | No | Historical |
| 63187-916-90 | 63187091690 | 90 TABLET in 1 BOTTLE (63187-916-90) | 90 tablet | 2017-09-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam Tablets, USP | Proficient Rx LP | 2019-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |