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"76282-239-10" National Drug Code (NDC)
Amlodipine Besylate 1000 TABLET in 1 BOTTLE (76282-239-10)
(Exelan Pharmaceuticals, Inc.)
NDC Code
76282-239-10
Package Description
1000 TABLET in 1 BOTTLE (76282-239-10)
Product NDC
76282-239
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20071102
Marketing Category Name
ANDA
Application Number
ANDA077955
Manufacturer
Exelan Pharmaceuticals, Inc.
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/76282-239-10