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"61786-202-19" National Drug Code (NDC)
Amlodipine Besylate 90 TABLET in 1 BOTTLE (61786-202-19)
(REMEDYREPACK INC.)
NDC Code
61786-202-19
Package Description
90 TABLET in 1 BOTTLE (61786-202-19)
Product NDC
61786-202
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20150602
Marketing Category Name
ANDA
Application Number
ANDA203245
Manufacturer
REMEDYREPACK INC.
Substance Name
AMLODIPINE BESYLATE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61786-202-19