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"51672-4057-6" National Drug Code (NDC)
Amiodarone Hydrochloride 30 TABLET in 1 BOTTLE (51672-4057-6)
(Taro Pharmaceuticals U.S.A., Inc.)
NDC Code
51672-4057-6
Package Description
30 TABLET in 1 BOTTLE (51672-4057-6)
Product NDC
51672-4057
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amiodarone Hydrochloride
Non-Proprietary Name
Amiodarone Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20021129
Marketing Category Name
ANDA
Application Number
ANDA076362
Manufacturer
Taro Pharmaceuticals U.S.A., Inc.
Substance Name
AMIODARONE HYDROCHLORIDE
Strength
400
Strength Unit
mg/1
Pharmacy Classes
Antiarrhythmic [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-4057-6