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"59762-2010-3" National Drug Code (NDC)
Amlodipine Besylate 300 TABLET in 1 BOTTLE (59762-2010-3)
(Greenstone LLC)
NDC Code
59762-2010-3
Package Description
300 TABLET in 1 BOTTLE (59762-2010-3)
Product NDC
59762-2010
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190624
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA019787
Manufacturer
Greenstone LLC
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/59762-2010-3