Alprazolam
- Product NDC
- 50090-2346
- 11-digit product format
- 500902346
- Labeler code
- 50090
- Product ID
- 50090-2346_902610ed-ad6e-4654-bc95-40972af75e4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record