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"52125-801-19" National Drug Code (NDC)
Amlodipine Besylate 90 TABLET in 1 BOTTLE (52125-801-19)
(REMEDYREPACK INC.)
NDC Code
52125-801-19
Package Description
90 TABLET in 1 BOTTLE (52125-801-19)
Product NDC
52125-801
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20131231
Marketing Category Name
ANDA
Application Number
ANDA078925
Manufacturer
REMEDYREPACK INC.
Substance Name
AMLODIPINE BESYLATE
Strength
2.5
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/52125-801-19