Diazepam
- Product NDC
- 63629-7328
- 11-digit product format
- 636297328
- Labeler code
- 63629
- Product ID
- 63629-7328_11b5ecf4-79a0-4390-a57d-5ac96d0f2ee3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071322
- Marketing category
- ANDA
- Marketing start
- 1986-12-10
- 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 |
|---|
| 63629-7328-1 | 63629732801 | 2 TABLET in 1 BOTTLE (63629-7328-1) | 2 tablet | 2017-07-20 | 0000-00-00 | No | No | Current |
| 63629-7328-2 | 63629732802 | 6 TABLET in 1 BOTTLE (63629-7328-2) | 6 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |