Amiodarone Hydrochloride 51672-4055-06

Package NDC

51672-4055-06

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]

Selected Package

51672-4055-06Selected

30 TABLET in 1 BOTTLE (51672-4055-6)