Diazepam
- Product NDC
- 68071-3270
- 11-digit product format
- 680713270
- Labeler code
- 68071
- Product ID
- 68071-3270_bb14f020-e55d-55bf-e053-2995a90af998
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA071135
- Marketing category
- ANDA
- Marketing start
- 2016-08-03
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3270-1 | 68071327001 | 10 TABLET in 1 BOTTLE (68071-3270-1) | 10 tablet | 2017-05-19 | 0000-00-00 | No | No | Current |
| 68071-3270-2 | 68071327002 | 2 TABLET in 1 BOTTLE (68071-3270-2) | 2 tablet | 2017-05-19 | 0000-00-00 | No | No | Current |
| 68071-3270-3 | 68071327003 | 3 TABLET in 1 BOTTLE (68071-3270-3) | 3 tablet | 2017-05-19 | 0000-00-00 | No | No | Current |
| 68071-3270-4 | 68071327004 | 4 TABLET in 1 BOTTLE (68071-3270-4) | 4 tablet | 2017-05-19 | 0000-00-00 | No | No | Current |
| 68071-3270-6 | 68071327006 | 6 TABLET in 1 BOTTLE (68071-3270-6) | 6 tablet | 2017-05-19 | 0000-00-00 | No | No | Current |