Diazepam
- Product NDC
- 66267-776
- 11-digit product format
- 662670776
- Labeler code
- 66267
- Product ID
- 66267-776_9cbd7b97-0846-e4e5-e053-2a95a90aefdd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA071135
- Marketing category
- ANDA
- Marketing start
- 1987-02-03
- 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
- 2021-12-31
- 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 |
|---|
| 66267-776-04 | 66267077604 | 4 TABLET in 1 BOTTLE (66267-776-04) | 4 tablet | 2017-01-24 | 0000-00-00 | No | No | Current |
| 66267-776-06 | 66267077606 | 6 TABLET in 1 BOTTLE (66267-776-06) | 6 tablet | 2017-01-24 | 0000-00-00 | No | No | Current |