"0185-0341-10" National Drug Code (NDC)

Fosinopril Sodium And Hydrochlorothiazide 1000 TABLET in 1 BOTTLE (0185-0341-10)
(Eon Labs, Inc.)

NDC Code0185-0341-10
Package Description1000 TABLET in 1 BOTTLE (0185-0341-10)
Product NDC0185-0341
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFosinopril Sodium And Hydrochlorothiazide
Non-Proprietary NameFosinopril Sodium And Hydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20050928
Marketing Category NameANDA
Application NumberANDA076961
ManufacturerEon Labs, Inc.
Substance NameFOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Strength10; 12.5
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

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