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"70518-3439-1" National Drug Code (NDC)
Amiodarone Hydrochloride 90 TABLET in 1 BOTTLE, PLASTIC (70518-3439-1)
(REMEDYREPACK INC.)
NDC Code
70518-3439-1
Package Description
90 TABLET in 1 BOTTLE, PLASTIC (70518-3439-1)
Product NDC
70518-3439
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amiodarone Hydrochloride
Non-Proprietary Name
Amiodarone Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20220614
Marketing Category Name
ANDA
Application Number
ANDA078578
Manufacturer
REMEDYREPACK 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 3A Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3439-1