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"70518-2632-3" National Drug Code (NDC)
Amlodipine Besylate 28 TABLET in 1 BLISTER PACK (70518-2632-3)
(REMEDYREPACK INC.)
NDC Code
70518-2632-3
Package Description
28 TABLET in 1 BLISTER PACK (70518-2632-3)
Product NDC
70518-2632
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200317
Marketing Category Name
ANDA
Application Number
ANDA078925
Manufacturer
REMEDYREPACK INC.
Substance Name
AMLODIPINE BESYLATE
Strength
10
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/70518-2632-3