"0185-0144-09" National Drug Code (NDC)

NDC Code	0185-0144-09
Package Description	90 TABLET in 1 BOTTLE (0185-0144-09)
Product NDC	0185-0144
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amiodarone Hydrochloride
Non-Proprietary Name	Amiodarone Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19981223
End Marketing Date	20220731
Marketing Category Name	ANDA
Application Number	ANDA075315
Manufacturer	Eon Labs, Inc.
Substance Name	AMIODARONE HYDROCHLORIDE
Strength	200
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 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]