Clonazepam
- Product NDC
- 68788-7181
- 11-digit product format
- 687887181
- Labeler code
- 68788
- Product ID
- 68788-7181_2a9e73d5-3777-45cb-996c-a3de7ccaadd6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA077147
- Marketing category
- ANDA
- Marketing start
- 2018-07-16
- 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 |
|---|
| 68788-7181-2 | 68788718102 | 20 TABLET in 1 BOTTLE, PLASTIC (68788-7181-2) | 20 tablet | 2018-07-16 | 0000-00-00 | No | No | Current |
| 68788-7181-3 | 68788718103 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-7181-3) | 30 tablet | 2018-07-16 | 0000-00-00 | No | No | Current |
| 68788-7181-6 | 68788718106 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-7181-6) | 60 tablet | 2018-07-16 | 0000-00-00 | No | No | Current |
| 68788-7181-9 | 68788718109 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-7181-9) | 90 tablet | 2018-07-16 | 0000-00-00 | No | No | Current |