Alprazolam
- Product NDC
- 0615-8000
- 11-digit product format
- 006158000
- Labeler code
- 0615
- Product ID
- 0615-8000_c372c1d1-5571-4941-ab48-bac0c9e989a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA074112
- Marketing category
- ANDA
- Marketing start
- 1995-12-29
- Marketing end
- 2020-02-29
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record