Diazepam
- Product NDC
- 50090-4713
- 11-digit product format
- 500904713
- Labeler code
- 50090
- Product ID
- 50090-4713_897e38ed-efe6-4dea-948e-79b22588f7e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071321
- Marketing category
- ANDA
- Marketing start
- 1986-12-10
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4713-0 | 50090471300 | 33 TABLET in 1 BOTTLE (50090-4713-0) | 33 tablet | 2019-11-12 | 0000-00-00 | No | No | Current |