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"70518-2132-3" National Drug Code (NDC)

Losartan Potassium 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2132-3)
(REMEDYREPACK INC.)

NDC Code70518-2132-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2132-3)
Product NDC70518-2132
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium
Non-Proprietary NameLosartan Potassium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190605
Marketing Category NameANDA
Application NumberANDA090083
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/70518-2132-3





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