Alprazolam
- Product NDC
- 70518-4137
- 11-digit product format
- 705184137
- Labeler code
- 70518
- Product ID
- 70518-4137_1cf8baf2-ee1d-a98b-e063-6394a90a0c81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074112
- Marketing category
- ANDA
- Marketing start
- 2024-07-10
- Marketing end
- 2027-03-19
- 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 |
|---|
| 70518-4137-0 | 70518413700 | 60 TABLET in 1 BOTTLE, PLASTIC (70518-4137-0) | 60 tablet | 2024-07-10 | 2027-03-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | REMEDYREPACK INC. | 2024-07-11 | HUMAN PRESCRIPTION DRUG LABEL | 1 |