Alprazolam
- Product NDC
- 63629-3308
- 11-digit product format
- 636293308
- Labeler code
- 63629
- Product ID
- 63629-3308_a372953f-4c60-4ac9-90b4-650e5f691b75
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018276
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1981-10-16
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#