Diazepam
- Product NDC
- 55154-7885
- 11-digit product format
- 551547885
- Labeler code
- 55154
- Product ID
- 55154-7885_f53a6f51-0d89-4295-ac85-4661129b631f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- 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
- 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 |
|---|
| 55154-7885-0 | 55154788500 | 10 BLISTER PACK in 1 BAG (55154-7885-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2008-06-05 | 0000-00-00 | No | No | Current |