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"21695-796-30" National Drug Code (NDC)
Amiodarone Hydrochloride 30 TABLET in 1 BOTTLE (21695-796-30)
(Rebel Distributors Corp)
NDC Code
21695-796-30
Package Description
30 TABLET in 1 BOTTLE (21695-796-30)
Product NDC
21695-796
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amiodarone Hydrochloride
Non-Proprietary Name
Amiodarone Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20090810
Marketing Category Name
ANDA
Application Number
ANDA079029
Manufacturer
Rebel Distributors Corp
Substance Name
AMIODARONE HYDROCHLORIDE
Strength
200
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]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/21695-796-30