Alprazolam
- Product NDC
- 0904-5858
- 11-digit product format
- 009045858
- Labeler code
- 0904
- Product ID
- 0904-5858_678e1530-a10b-4f16-a3d4-c7aa12359799
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 2008-04-02
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record