Clonazepam
- Product NDC
- 70518-3891
- 11-digit product format
- 705183891
- Labeler code
- 70518
- Product ID
- 70518-3891_3b2aa260-0636-7a25-e063-6294a90a3a89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075468
- Marketing category
- ANDA
- Marketing start
- 2023-10-10
- 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 |
|---|
| 70518-3891-0 | 70518389100 | 30 TABLET in 1 BLISTER PACK (70518-3891-0) | 30 tablet | 2023-10-10 | No | No | Historical |
| 70518-3891-1 | 70518389101 | 100 POUCH in 1 BOX (70518-3891-1) / 1 TABLET in 1 POUCH (70518-3891-2) | 100 pouch | 2023-10-19 | No | No | Historical |
| 70518-3891-3 | 70518389103 | 100 POUCH in 1 BOX (70518-3891-3) / 1 TABLET in 1 POUCH (70518-3891-4) | 100 pouch | 2025-01-07 | No | No | Historical |