Diazepam
- Product NDC
- 68788-8281
- 11-digit product format
- 687888281
- Labeler code
- 68788
- Product ID
- 68788-8281_9e34adca-3182-4d86-a51c-9b28a130268a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA071135
- Marketing category
- ANDA
- Marketing start
- 2022-11-04
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8281 | DIAZEPAM TABLET [PREFERRED PHARMACEUTICALS INC.] | 3 | Legacy NDC | 20240410_9e34adca-3182-4d86-a51c-9b28a130268a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8281-1 | 68788828101 | 15 TABLET in 1 BOTTLE, PLASTIC (68788-8281-1) | 15 tablet | 2022-11-04 | 0000-00-00 | No | No | Current |
| 68788-8281-2 | 68788828102 | 20 TABLET in 1 BOTTLE, PLASTIC (68788-8281-2) | 20 tablet | 2022-11-04 | 0000-00-00 | No | No | Current |
| 68788-8281-3 | 68788828103 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-8281-3) | 30 tablet | 2022-11-04 | 0000-00-00 | No | No | Current |
| 68788-8281-6 | 68788828106 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-8281-6) | 60 tablet | 2022-11-04 | 0000-00-00 | No | No | Current |
| 68788-8281-8 | 68788828108 | 100 TABLET in 1 BOTTLE, PLASTIC (68788-8281-8) | 100 tablet | 2022-11-04 | 0000-00-00 | No | No | Current |
| 68788-8281-9 | 68788828109 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-8281-9) | 90 tablet | 2022-11-04 | 0000-00-00 | No | No | Current |