"65862-837-05" National Drug Code (NDC)

Amlodipine, Valsartan And Hydrochlorothiazide 500 TABLET, FILM COATED in 1 BOTTLE (65862-837-05)
(Aurobindo Pharma Limited)

NDC Code65862-837-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (65862-837-05)
Product NDC65862-837
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine, Valsartan And Hydrochlorothiazide
Non-Proprietary NameAmlodipine, Valsartan And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171219
Marketing Category NameANDA
Application NumberANDA206180
ManufacturerAurobindo Pharma Limited
Substance NameAMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN
Strength10; 25; 160
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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