Clonazepam
- Product NDC
- 51079-882
- 11-digit product format
- 510790882
- Labeler code
- 51079
- Product ID
- 51079-882_7df4a15f-f1ab-7cb1-e053-2991aa0acde5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA075150
- Marketing category
- ANDA
- Marketing start
- 1997-07-15
- Marketing end
- 2020-02-29
- Substance
- CLONAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record