Amiodarone Hydrochloride 51672-4056-06

Package NDC

51672-4056-06

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]

Selected Package

51672-4056-06Selected

30 TABLET in 1 BOTTLE (51672-4056-6)

Other packages for this product(2)

51672-4056-01

100 TABLET in 1 BOTTLE (51672-4056-1)

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51672-4056-03

1000 TABLET in 1 BOTTLE (51672-4056-3)

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