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"71335-0890-3" National Drug Code (NDC)
Amlodipine Besylate 120 TABLET in 1 BOTTLE (71335-0890-3)
(Bryant Ranch Prepack)
NDC Code
71335-0890-3
Package Description
120 TABLET in 1 BOTTLE (71335-0890-3)
Product NDC
71335-0890
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
Bryant Ranch Prepack
Substance Name
AMLODIPINE BESYLATE
Strength
2.5
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/71335-0890-3