Alprazolam
- Product NDC
- 55700-491
- 11-digit product format
- 557000491
- Labeler code
- 55700
- Product ID
- 55700-491_48d6cb0f-e347-4649-8628-15434b4373c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA200739
- Marketing category
- ANDA
- Marketing start
- 2017-01-27
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 1 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