Diazepam
- Product NDC
- 0615-7800
- 11-digit product format
- 006157800
- Labeler code
- 0615
- Product ID
- 0615-7800_5f67e957-148a-467c-bcf9-086a40c4f9b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA071322
- Marketing category
- ANDA
- Marketing start
- 1986-12-10
- Marketing end
- 2023-08-31
- Substance
- DIAZEPAM
- Active strength
- 10 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0615-7800-39 | 00615780039 | 30 TABLET in 1 BLISTER PACK (0615-7800-39) | 30 tablet | 2016-04-27 | 2023-08-31 | No | No | Current |