Diazepam
- Product NDC
- 68071-2828
- 11-digit product format
- 680712828
- Labeler code
- 68071
- Product ID
- 68071-2828_e8a58ea4-bce5-3625-e053-2a95a90a173d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA071135
- Marketing category
- ANDA
- Marketing start
- 2019-10-31
- 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 |
|---|
| 68071-2828-3 | 68071282803 | 30 TABLET in 1 BOTTLE, PLASTIC (68071-2828-3) | 30 tablet | 2022-09-14 | 0000-00-00 | No | No | Current |