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"70518-1319-0" National Drug Code (NDC)

Losartan Potassium 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1319-0)
(REMEDYREPACK INC.)

NDC Code70518-1319-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1319-0)
Product NDC70518-1319
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium
Non-Proprietary NameLosartan Potassium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180724
Marketing Category NameANDA
Application NumberANDA078243
ManufacturerREMEDYREPACK INC.
Substance NameLOSARTAN POTASSIUM
Strength25
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1319-0





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