"68180-772-09" National Drug Code (NDC)

Amlodipine, Valsartan And Hydrochlorothiazide 90 TABLET, FILM COATED in 1 BOTTLE (68180-772-09)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-772-09
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68180-772-09)
Product NDC68180-772
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine, Valsartan And Hydrochlorothiazide
Non-Proprietary NameAmlodipine, Valsartan And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150604
Marketing Category NameANDA
Application NumberANDA200797
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameAMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN
Strength10; 12.5; 160
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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