Diazepam
- Product NDC
- 68788-9208
- 11-digit product format
- 687889208
- Labeler code
- 68788
- Product ID
- 68788-9208_2dfc070f-6536-456b-af68-57177158fe06
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA071321
- Marketing category
- ANDA
- Marketing start
- 2011-11-09
- 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
- 2022-12-31
- 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 |
|---|
| 68788-9208-0 | 68788920800 | 2 TABLET in 1 BOTTLE (68788-9208-0) | 2 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |
| 68788-9208-1 | 68788920801 | 15 TABLET in 1 BOTTLE (68788-9208-1) | 15 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |
| 68788-9208-2 | 68788920802 | 20 TABLET in 1 BOTTLE (68788-9208-2) | 20 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |
| 68788-9208-3 | 68788920803 | 30 TABLET in 1 BOTTLE (68788-9208-3) | 30 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |
| 68788-9208-4 | 68788920804 | 10 TABLET in 1 BOTTLE (68788-9208-4) | 10 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |
| 68788-9208-5 | 68788920805 | 6 TABLET in 1 BOTTLE (68788-9208-5) | 6 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |
| 68788-9208-6 | 68788920806 | 60 TABLET in 1 BOTTLE (68788-9208-6) | 60 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |
| 68788-9208-8 | 68788920808 | 100 TABLET in 1 BOTTLE (68788-9208-8) | 100 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |
| 68788-9208-9 | 68788920809 | 90 TABLET in 1 BOTTLE (68788-9208-9) | 90 tablet | 2011-11-09 | 0000-00-00 | No | No | Current |