Clonazepam
- Product NDC
- 72189-475
- 11-digit product format
- 721890475
- Labeler code
- 72189
- Product ID
- 72189-475_2c4e05d7-5e1c-f566-e063-6294a90acada
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA077856
- Marketing category
- ANDA
- Marketing start
- 2023-05-24
- Substance
- CLONAZEPAM
- Active strength
- 1 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 |
|---|
| 72189-475-30 | 72189047530 | 30 TABLET in 1 BOTTLE (72189-475-30) | 30 tablet | 2023-05-24 | No | No | Historical |
| 72189-475-60 | 72189047560 | 60 TABLET in 1 BOTTLE (72189-475-60) | 60 tablet | 2023-05-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Clonazepam | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 2 |