Alprazolam
- Product NDC
- 50090-7556
- 11-digit product format
- 500907556
- Labeler code
- 50090
- Product ID
- 50090-7556_271e876d-55ae-4f6b-bf83-532298722dd9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090871
- Marketing category
- ANDA
- Marketing start
- 2011-06-07
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7556-1 | 50090755601 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7556-1) | 2025-05-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | A-S Medication Solutions | 2025-05-28 | Human Prescription Drug Label | 1 |