Diazepam
- Product NDC
- 50436-3593
- 11-digit product format
- 504363593
- Labeler code
- 50436
- Product ID
- 50436-3593_dd6b33ce-17c8-45f6-90c7-35bbc2a6dfb3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077749
- Marketing category
- ANDA
- Marketing start
- 2006-03-31
- Marketing end
- 2019-08-31
- Substance
- DIAZEPAM
- Active strength
- 10 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