Clonazepam
- Product NDC
- 68071-3613
- 11-digit product format
- 680713613
- Labeler code
- 68071
- Product ID
- 68071-3613_19b1f515-5241-e6b9-e063-6394a90a7c2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077856
- Marketing category
- ANDA
- Marketing start
- 2018-02-15
- Substance
- CLONAZEPAM
- Active strength
- 2 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 |
|---|
| 68071-3613-6 | 68071361306 | 60 TABLET in 1 BOTTLE, PLASTIC (68071-3613-6) | 60 tablet | 2024-05-30 | No | No | Historical |