Clonazepam
- Product NDC
- 63629-7649
- 11-digit product format
- 636297649
- Labeler code
- 63629
- Product ID
- 63629-7649_7a5669e7-b782-4947-91b2-7bba091499af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077147
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- Marketing end
- 0000-00-00
- Substance
- CLONAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-7649-1 | 63629764901 | 30 TABLET in 1 BOTTLE (63629-7649-1) | 30 tablet | 2018-05-30 | 0000-00-00 | No | No | Current |
| 63629-7649-2 | 63629764902 | 60 TABLET in 1 BOTTLE (63629-7649-2) | 60 tablet | 2021-12-23 | 0000-00-00 | No | No | Current |