Diazepam
- Product NDC
- 80425-0151
- 11-digit product format
- 804250151
- Labeler code
- 80425
- Product ID
- 80425-0151_ed0e31e3-f44e-eb81-e053-2995a90aaf61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- ANDA071136
- Marketing category
- ANDA
- Marketing start
- 2019-10-31
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 10 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80425-0151-2 | 80425015102 | 60 TABLET in 1 BOTTLE (80425-0151-2) | 60 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |