Diazepam
- Product NDC
- 63629-7851
- 11-digit product format
- 636297851
- Labeler code
- 63629
- Product ID
- 63629-7851_bb003043-e597-4d77-a001-eb1016b25f1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071321
- Marketing category
- ANDA
- Marketing start
- 1986-12-10
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 5 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-7851-1 | 63629785101 | 10 TABLET in 1 BOTTLE (63629-7851-1) | 10 tablet | 2005-07-27 | 0000-00-00 | No | No | Current |