Diazepam
- Product NDC
- 68788-7452
- 11-digit product format
- 687887452
- Labeler code
- 68788
- Product ID
- 68788-7452_04afe522-25a0-4436-90e7-f17cf4bb908a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- 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
- 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 |
|---|
| 68788-7452-1 | 68788745201 | 15 TABLET in 1 BOTTLE (68788-7452-1) | 15 tablet | 2019-12-31 | 0000-00-00 | No | No | Current |
| 68788-7452-2 | 68788745202 | 20 TABLET in 1 BOTTLE (68788-7452-2) | 20 tablet | 2019-12-31 | 0000-00-00 | No | No | Current |
| 68788-7452-3 | 68788745203 | 30 TABLET in 1 BOTTLE (68788-7452-3) | 30 tablet | 2019-12-31 | 0000-00-00 | No | No | Current |
| 68788-7452-6 | 68788745206 | 60 TABLET in 1 BOTTLE (68788-7452-6) | 60 tablet | 2019-12-31 | 0000-00-00 | No | No | Current |
| 68788-7452-8 | 68788745208 | 100 TABLET in 1 BOTTLE (68788-7452-8) | 100 tablet | 2019-12-31 | 0000-00-00 | No | No | Current |
| 68788-7452-9 | 68788745209 | 90 TABLET in 1 BOTTLE (68788-7452-9) | 90 tablet | 2019-12-31 | 0000-00-00 | No | No | Current |