Clonazepam
- Product NDC
- 71205-529
- 11-digit product format
- 712050529
- Labeler code
- 71205
- Product ID
- 71205-529_63286201-4b79-45b8-8f48-7e21dadc1408
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077856
- Marketing category
- ANDA
- Marketing start
- 2018-02-15
- 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 |
|---|
| 71205-529-30 | 71205052930 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-529-30) | 30 tablet | 2021-02-02 | No | No | Historical |
| 71205-529-60 | 71205052960 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-529-60) | 60 tablet | 2021-02-02 | No | No | Historical |
| 71205-529-90 | 71205052990 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-529-90) | 90 tablet | 2021-02-02 | No | No | Historical |