Diazepam
- Product NDC
- 0904-5880
- 11-digit product format
- 009045880
- Labeler code
- 0904
- Product ID
- 0904-5880_2fa9bfb9-0e7e-457d-af69-5cfd5c50347b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA071135
- Marketing category
- ANDA
- Marketing start
- 2008-06-05
- 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
- 2020-12-31
- 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 |
|---|
| 0904-5880-61 | 00904588061 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5880-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2008-06-05 | 0000-00-00 | No | No | Current |