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"70518-2981-5" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BLISTER PACK (70518-2981-5)
(REMEDYREPACK INC.)
NDC Code
70518-2981-5
Package Description
30 TABLET in 1 BLISTER PACK (70518-2981-5)
Product NDC
70518-2981
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20210106
Marketing Category Name
ANDA
Application Number
ANDA078925
Manufacturer
REMEDYREPACK INC.
Substance Name
AMLODIPINE BESYLATE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2981-5