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"61919-782-30" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BOTTLE (61919-782-30)
(Direct_Rx)
NDC Code
61919-782-30
Package Description
30 TABLET in 1 BOTTLE (61919-782-30)
Product NDC
61919-782
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190729
Marketing Category Name
ANDA
Application Number
ANDA203245
Manufacturer
Direct_Rx
Substance Name
AMLODIPINE BESYLATE
Strength
10
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/61919-782-30