Clonazepam
- Product NDC
- 71335-2653
- 11-digit product format
- 713352653
- Labeler code
- 71335
- Product ID
- 71335-2653_109c2b88-9bf1-4537-aab1-16e804fcb49a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075150
- Marketing category
- ANDA
- Marketing start
- 2023-01-17
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Clonazepam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CLONAZEPAM | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5PE9FDE8GB |
| Rxcui | 197529 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2653-1 | 71335265301 | 30 TABLET in 1 BOTTLE (71335-2653-1) | 30 tablet | 2025-06-20 | No | No | Historical |
| 71335-2653-2 | 71335265302 | 60 TABLET in 1 BOTTLE (71335-2653-2) | 60 tablet | 2025-06-20 | No | No | Historical |
| 71335-2653-3 | 71335265303 | 90 TABLET in 1 BOTTLE (71335-2653-3) | 90 tablet | 2025-06-20 | No | No | Historical |
| 71335-2653-4 | 71335265304 | 120 TABLET in 1 BOTTLE (71335-2653-4) | 120 tablet | 2025-06-20 | No | No | Historical |
| 71335-2653-5 | 71335265305 | 10 TABLET in 1 BOTTLE (71335-2653-5) | 10 tablet | 2025-06-20 | No | No | Historical |
| 71335-2653-6 | 71335265306 | 180 TABLET in 1 BOTTLE (71335-2653-6) | 180 tablet | 2025-06-20 | No | No | Historical |