Clonazepam
- Product NDC
- 0185-0064
- 11-digit product format
- 001850064
- Labeler code
- 0185
- Product ID
- 0185-0064_54b73287-b172-4b78-ac53-87a187ae594f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA074979
- Marketing category
- ANDA
- Marketing start
- 1997-08-29
- Marketing end
- 2021-04-30
- 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0185-0064-01 | 00185006401 | 100 TABLET in 1 BOTTLE (0185-0064-01) | 100 tablet | 1997-08-29 | 2021-04-30 | No | No | Current |
| 0185-0064-05 | 00185006405 | 500 TABLET in 1 BOTTLE (0185-0064-05) | 500 tablet | 1997-08-29 | 2021-04-30 | No | No | Current |
| 0185-0064-10 | 00185006410 | 1000 TABLET in 1 BOTTLE (0185-0064-10) | 1000 tablet | 1997-08-29 | 2021-04-30 | No | No | Current |