Diazepam
- Product NDC
- 63629-8192
- 11-digit product format
- 636298192
- Labeler code
- 63629
- Product ID
- 63629-8192_c26f75c8-0156-4392-a0bd-a155328a2f22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 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 |
|---|
| 63629-8192-1 | 63629819201 | 10 TABLET in 1 BOTTLE (63629-8192-1) | 10 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8192-2 | 63629819202 | 30 TABLET in 1 BOTTLE (63629-8192-2) | 30 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |