Clorazepate Dipotassium
- Product NDC
- 67046-1501
- 11-digit product format
- 670461501
- Labeler code
- 67046
- Product ID
- 67046-1501_2ccafa6f-08ea-91c7-e063-6294a90aa353
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clorazepate Dipotassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA075731
- Marketing category
- ANDA
- Marketing start
- 2025-01-28
- Substance
- CLORAZEPATE DIPOTASSIUM
- Active strength
- 15 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 63FN7G03XY | CLORAZEPATE DIPOTASSIUM | 57109-90-7 | CLORAZEPATE DIPOTASSIUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-1501-3 | 67046150103 | 30 TABLET in 1 BLISTER PACK (67046-1501-3) | 30 tablet | 2025-01-28 | No | No | Historical |