Diazepam
- Product NDC
- 0615-7799
- 11-digit product format
- 006157799
- Labeler code
- 0615
- Product ID
- 0615-7799_3fde064b-ba25-419a-b560-710f6c889e33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA071321
- Marketing category
- ANDA
- Marketing start
- 1986-12-10
- Marketing end
- 2023-10-31
- Substance
- DIAZEPAM
- Active strength
- 5 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 |
|---|
| 0615-7799-39 | 00615779939 | 30 TABLET in 1 BLISTER PACK (0615-7799-39) | 30 tablet | 2019-03-11 | 2023-10-31 | No | No | Current |