Diazepam
- Product NDC
- 0093-6137
- 11-digit product format
- 000936137
- Labeler code
- 0093
- Product ID
- 0093-6137_197afffd-f745-4906-a173-9b10b5ba84ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- GEL
- Route
- RECTAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- NDA020648
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2010-10-01
- Marketing end
- 2020-10-31
- Substance
- DIAZEPAM
- Active strength
- 3 mg/.5mL
- 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