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"61919-732-90" National Drug Code (NDC)

Losartan Potassium Hctz 90 TABLET, FILM COATED in 1 BOTTLE (61919-732-90)
(DIRECT RX)

NDC Code61919-732-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61919-732-90)
Product NDC61919-732
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium Hctz
Non-Proprietary NameLosartan Potassium Hctz
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190418
Marketing Category NameANDA
Application NumberANDA091629
ManufacturerDIRECT RX
Substance NameHYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength12.5; 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/61919-732-90





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