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"61786-819-02" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BOTTLE (61786-819-02)
(REMEDYREPACK INC.)
NDC Code
61786-819-02
Package Description
30 TABLET in 1 BOTTLE (61786-819-02)
Product NDC
61786-819
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160815
Marketing Category Name
ANDA
Application Number
ANDA203245
Manufacturer
REMEDYREPACK INC.
Substance Name
AMLODIPINE BESYLATE
Strength
10
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/61786-819-02