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"65862-103-05" National Drug Code (NDC)
Amlodipine Besylate 500 TABLET in 1 BOTTLE (65862-103-05)
(Aurobindo Pharma Limited)
NDC Code
65862-103-05
Package Description
500 TABLET in 1 BOTTLE (65862-103-05)
Product NDC
65862-103
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070717
Marketing Category Name
ANDA
Application Number
ANDA078021
Manufacturer
Aurobindo Pharma Limited
Substance Name
AMLODIPINE BESYLATE
Strength
10
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/65862-103-05