"68382-142-06" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 30 TABLET, FILM COATED in 1 BOTTLE (68382-142-06)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-142-06
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68382-142-06)
Product NDC68382-142
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20101004
Marketing Category NameANDA
Application NumberANDA078385
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameHYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength12.5; 50
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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