Alprazolam
- Product NDC
- 60760-678
- 11-digit product format
- 607600678
- Labeler code
- 60760
- Product ID
- 60760-678_fc5fe7a0-42ee-b1c8-e053-6394a90a020c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA203346
- Marketing category
- ANDA
- Marketing start
- 2015-07-31
- Substance
- ALPRAZOLAM
- Active strength
- 1 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 |
|---|
| 60760-678-30 | 60760067830 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-678-30) | 30 tablet | 2023-05-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | ST. MARY'S MEDICAL PARK PHARMACY | 2023-05-23 | HUMAN PRESCRIPTION DRUG LABEL | 1 |