"68382-143-10" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 1000 TABLET, FILM COATED in 1 BOTTLE (68382-143-10)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-143-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (68382-143-10)
Product NDC68382-143
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
Strength25; 100
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-143-10