Clonazepam
- Product NDC
- 71335-1810
- 11-digit product format
- 713351810
- Labeler code
- 71335
- Product ID
- 71335-1810_530f1279-3174-4088-963c-e8cda62663f9
- 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 |
|---|
| 71335-1810-1 | 71335181001 | 20 TABLET in 1 BOTTLE, PLASTIC (71335-1810-1) | 20 tablet | 2021-03-29 | No | No | Historical |
| 71335-1810-2 | 71335181002 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-1810-2) | 30 tablet | 2021-03-29 | No | No | Historical |
| 71335-1810-3 | 71335181003 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-1810-3) | 60 tablet | 2021-03-29 | No | No | Historical |
| 71335-1810-4 | 71335181004 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-1810-4) | 90 tablet | 2021-03-29 | No | No | Historical |
| 71335-1810-5 | 71335181005 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-1810-5) | 120 tablet | 2021-03-29 | No | No | Historical |
| 71335-1810-6 | 71335181006 | 56 TABLET in 1 BOTTLE, PLASTIC (71335-1810-6) | 56 tablet | 2021-03-29 | No | No | Historical |
| 71335-1810-7 | 71335181007 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-1810-7) | 28 tablet | 2021-03-29 | No | No | Historical |
| 71335-1810-8 | 71335181008 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-1810-8) | 100 tablet | 2021-03-29 | No | No | Historical |
| 71335-1810-9 | 71335181009 | 45 TABLET in 1 BOTTLE, PLASTIC (71335-1810-9) | 45 tablet | 2021-03-29 | No | No | Historical |