Amiodarone Hydrochloride 51672-4055
Product NDC
51672-4055- 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 | 100 mg/1 |
Drug Class
Antiarrhythmic [EPC]Cytochrome P450 1A2 Inhibitors [MoA]Cytochrome P450 2C9 Inhibitors [MoA]
Packaging Options(1)
30 TABLET in 1 BOTTLE (51672-4055-6)