Clonazepam
- Product NDC
- 70518-1559
- 11-digit product format
- 705181559
- Labeler code
- 70518
- Product ID
- 70518-1559_e56d7484-18c7-5403-e053-2995a90a410e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077147
- Marketing category
- ANDA
- Marketing start
- 2018-10-19
- Marketing end
- 0000-00-00
- Substance
- CLONAZEPAM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1559-1 | 70518155901 | 100 POUCH in 1 BOX (70518-1559-1) > 1 TABLET in 1 POUCH (70518-1559-2) | 100 pouch | 2019-06-12 | 0000-00-00 | No | No | Current |