Alprazolam
- Product NDC
- 43063-828
- 11-digit product format
- 430630828
- Labeler code
- 43063
- Product ID
- 43063-828_9d38d4a3-0c29-0934-e053-2a95a90a941b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA074174
- Marketing category
- ANDA
- Marketing start
- 2007-03-28
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record