Amiodarone Hydrochloride 51672-4025-02
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 30, 2001
- Listing Expires
- December 31, 2027
- Application
- ANDA075424
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amiodarone Hydrochloride | 200 mg/1 |
Drug Class
Antiarrhythmic [EPC]Cytochrome P450 1A2 Inhibitors [MoA]Cytochrome P450 2C9 Inhibitors [MoA]
Selected Package
51672-4025-02Selected500 TABLET in 1 BOTTLE (51672-4025-2)
Other packages for this product(2)
1000 TABLET in 1 BOTTLE (51672-4025-3)
60 TABLET in 1 BOTTLE (51672-4025-4)