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"61786-309-31" National Drug Code (NDC)
Amiodarone Hydrochloride 500 TABLET in 1 BOTTLE (61786-309-31)
(REMEDYREPACK INC.)
NDC Code
61786-309-31
Package Description
500 TABLET in 1 BOTTLE (61786-309-31)
Product NDC
61786-309
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amiodarone Hydrochloride
Non-Proprietary Name
Amiodarone Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20150512
Marketing Category Name
ANDA
Application Number
ANDA075315
Manufacturer
REMEDYREPACK INC.
Substance Name
AMIODARONE HYDROCHLORIDE
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Antiarrhythmic [EPC],Cytochrome P450 3A4 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Cytochrome P450 1A2 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61786-309-31