Alprazolam
- Product NDC
- 71205-652
- 11-digit product format
- 712050652
- Labeler code
- 71205
- Product ID
- 71205-652_4579facb-b225-4108-a5ef-dada926ef7cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA018276
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1981-10-16
- Substance
- ALPRAZOLAM
- Active strength
- .5 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 |
|---|
| 71205-652-30 | 71205065230 | 30 TABLET in 1 BOTTLE (71205-652-30) | 30 tablet | 2022-04-12 | No | No | Historical |
| 71205-652-60 | 71205065260 | 60 TABLET in 1 BOTTLE (71205-652-60) | 60 tablet | 2022-04-12 | No | No | Historical |
| 71205-652-90 | 71205065290 | 90 TABLET in 1 BOTTLE (71205-652-90) | 90 tablet | 2022-04-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | Proficient Rx LP | 2022-04-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |