Clonazepam
- Product NDC
- 16714-750
- 11-digit product format
- 167140750
- Labeler code
- 16714
- Product ID
- 16714-750_e76a8afe-0b3b-4ec0-8a16-ccb4a7f15d29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northstar RxLLC
- Application
- ANDA074979
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- Marketing end
- 2021-11-30
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-750-01 | 16714075001 | 100 TABLET in 1 BOTTLE (16714-750-01) | 100 tablet | 2017-09-01 | 2021-11-30 | No | No | Current |
| 16714-750-02 | 16714075002 | 500 TABLET in 1 BOTTLE (16714-750-02) | 500 tablet | 2017-09-01 | 2021-11-30 | No | No | Current |