Amiodarone Hydrochloride 51672-4057-06
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 29, 2002
- Listing Expires
- December 31, 2027
- Application
- ANDA076362
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amiodarone Hydrochloride | 400 mg/1 |
Drug Class
Antiarrhythmic [EPC]Cytochrome P450 1A2 Inhibitors [MoA]Cytochrome P450 2C9 Inhibitors [MoA]
Selected Package
51672-4057-06Selected30 TABLET in 1 BOTTLE (51672-4057-6)
Other packages for this product(1)
10 BLISTER PACK in 1 CARTON (51672-4057-0) / 10 TABLET in 1 BLISTER PACK