Clonazepam
- Product NDC
- 43063-788
- 11-digit product format
- 430630788
- Labeler code
- 43063
- Product ID
- 43063-788_414bb263-b84a-5358-e063-6294a90ad4bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA077147
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- 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 |
|---|
| 43063-788-30 | 43063078830 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-788-30) | 30 tablet | 2017-09-01 | No | No | Historical |