Diazepam
- Product NDC
- 67296-0084
- 11-digit product format
- 672960084
- Labeler code
- 67296
- Product ID
- 67296-0084_e688ebde-868b-a063-e053-2995a90a4874
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA071321
- Marketing category
- ANDA
- Marketing start
- 2013-01-01
- 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0084 | DIAZEPAM TABLET [REDPHARM DRUG, INC.] | 8 | Legacy NDC, 6 package rows | 20240612_41d6e67d-3ae5-6aba-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-0084-1 | 67296008401 | 15 TABLET in 1 BOTTLE (67296-0084-1) | 15 tablet | 2013-01-01 | 0000-00-00 | No | No | Current |
| 67296-0084-2 | 67296008402 | 2 TABLET in 1 BOTTLE (67296-0084-2) | 2 tablet | 2013-01-01 | 0000-00-00 | No | No | Current |
| 67296-0084-3 | 67296008403 | 10 TABLET in 1 BOTTLE (67296-0084-3) | 10 tablet | 2013-01-01 | 0000-00-00 | No | No | Current |
| 67296-0084-4 | 67296008404 | 20 TABLET in 1 BOTTLE (67296-0084-4) | 20 tablet | 2013-01-01 | 0000-00-00 | No | No | Current |
| 67296-0084-5 | 67296008405 | 4 TABLET in 1 BOTTLE (67296-0084-5) | 4 tablet | 2013-01-01 | 0000-00-00 | No | No | Current |
| 67296-0084-6 | 67296008406 | 6 TABLET in 1 BOTTLE (67296-0084-6) | 6 tablet | 2013-01-01 | 0000-00-00 | No | No | Current |