Alprazolam
- Product NDC
- 66267-013
- 11-digit product format
- 662670013
- Labeler code
- 66267
- Product ID
- 66267-013_9cbdbe41-12e1-6938-e053-2a95a90ae941
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA074112
- Marketing category
- ANDA
- Marketing start
- 2016-09-21
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record