Clorazepate Dipotassium 51672-4043
Product NDC
51672-4043- Manufacturer
- Taro Pharmaceuticals U.s.a., Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- April 27, 2000
- Listing Expires
- December 31, 2026
- Application
- ANDA075731
Active Ingredients
| Ingredient | Strength |
|---|---|
| Clorazepate Dipotassium | 7.5 mg/1 |
Drug Class
Benzodiazepine [EPC]Benzodiazepines [CS]
Packaging Options(3)
100 TABLET in 1 BOTTLE (51672-4043-1)
500 TABLET in 1 BOTTLE (51672-4043-2)
1000 TABLET in 1 BOTTLE (51672-4043-3)