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"59762-1530-4" National Drug Code (NDC)
Amlodipine Besylate 2500 TABLET in 1 BOTTLE (59762-1530-4)
(Greenstone LLC)
NDC Code
59762-1530-4
Package Description
2500 TABLET in 1 BOTTLE (59762-1530-4)
Product NDC
59762-1530
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070323
End Marketing Date
20200331
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],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59762-1530-4