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"42708-066-30" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BOTTLE (42708-066-30)
(QPharma Inc)
NDC Code
42708-066-30
Package Description
30 TABLET in 1 BOTTLE (42708-066-30)
Product NDC
42708-066
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20101020
Marketing Category Name
ANDA
Application Number
ANDA078925
Manufacturer
QPharma Inc
Substance Name
AMLODIPINE BESYLATE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/42708-066-30