Clonazepam
- Product NDC
- 50090-5399
- 11-digit product format
- 500905399
- Labeler code
- 50090
- Product ID
- 50090-5399_4a7c92f5-8663-4892-8182-cdb17772b6f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077147
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- 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
- 2022-12-31
- 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 |
|---|
| 50090-5399-0 | 50090539900 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-5399-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2020-12-04 | 0000-00-00 | No | No | Current |