Clonazepam
- Product NDC
- 70518-2152
- 11-digit product format
- 705182152
- Labeler code
- 70518
- Product ID
- 70518-2152_8c420a34-8a4c-5b85-e053-2995a90a70cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074869
- Marketing category
- ANDA
- Marketing start
- 2019-06-25
- Marketing end
- 0000-00-00
- Substance
- CLONAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record