Amiodarone Hydrochloride 51672-4056
Product NDC
51672-4056- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 2, 2003
- Listing Expires
- December 31, 2027
- Application
- ANDA076362
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amiodarone Hydrochloride | 300 mg/1 |
Drug Class
Antiarrhythmic [EPC]Cytochrome P450 1A2 Inhibitors [MoA]Cytochrome P450 2C9 Inhibitors [MoA]
Packaging Options(3)
100 TABLET in 1 BOTTLE (51672-4056-1)
1000 TABLET in 1 BOTTLE (51672-4056-3)
30 TABLET in 1 BOTTLE (51672-4056-6)