Clonazepam
- Product NDC
- 50090-4841
- 11-digit product format
- 500904841
- Labeler code
- 50090
- Product ID
- 50090-4841_fc41511e-6c8b-48c9-a090-f14ff917288f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074569
- Marketing category
- ANDA
- Marketing start
- 1996-09-18
- 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 |
|---|
| 50090-4841-2 | 50090484102 | 90 TABLET in 1 BOTTLE (50090-4841-2) | 90 tablet | 2020-01-20 | No | No | Historical |