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"52605-042-19" National Drug Code (NDC)
Amlodipine Besylate 90 TABLET in 1 BOTTLE (52605-042-19)
(POLYGEN PHARMACEUTICALS INC.)
NDC Code
52605-042-19
Package Description
90 TABLET in 1 BOTTLE (52605-042-19)
Product NDC
52605-042
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160711
Marketing Category Name
ANDA
Application Number
ANDA207821
Manufacturer
POLYGEN PHARMACEUTICALS 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/52605-042-19