Clonazepam
- Product NDC
- 63629-1201
- 11-digit product format
- 636291201
- Labeler code
- 63629
- Product ID
- 63629-1201_405c66a0-a25c-4553-8cdd-ce6d39a9ae32
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077856
- Marketing category
- ANDA
- Marketing start
- 2018-02-15
- Substance
- CLONAZEPAM
- Active strength
- .5 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5PE9FDE8GB | CLONAZEPAM | 1622-61-3 | CLONAZEPAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-1201-1 | 63629120101 | 500 TABLET in 1 BOTTLE (63629-1201-1) | 500 tablet | 2021-01-14 | No | No | Historical |