"51862-156-30" National Drug Code (NDC)

NDC Code	51862-156-30
Package Description	30 TABLET in 1 BOTTLE (51862-156-30)
Product NDC	51862-156
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amiodarone Hcl
Non-Proprietary Name	Amiodarone Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130101
End Marketing Date	20191231
Marketing Category Name	ANDA
Application Number	ANDA077069
Manufacturer	Mayne Pharma Inc.
Substance Name	AMIODARONE HYDROCHLORIDE
Strength	400
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA],Antiarrhythmic [EPC],Cytochrome P450 3A4 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Cytochrome P450 1A2 Inhibitors [MoA]