Diazepam
- Product NDC
- 51862-064
- 11-digit product format
- 518620064
- Labeler code
- 51862
- Product ID
- 51862-064_49cd2631-74e5-4291-a491-b15b2fa31ee3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mayne Pharma
- Application
- ANDA071136
- Marketing category
- ANDA
- Marketing start
- 2016-08-03
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 10 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51862-064-05 | 51862006405 | 500 TABLET in 1 BOTTLE, PLASTIC (51862-064-05) | 500 tablet | 2016-08-03 | 0000-00-00 | No | No | Current |