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"16571-502-30" National Drug Code (NDC)

Losartan Potassium 30 TABLET, FILM COATED in 1 BOTTLE (16571-502-30)
(Rising Pharmaceuticals, Inc)

NDC Code16571-502-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (16571-502-30)
Product NDC16571-502
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium
Non-Proprietary NameLosartan Potassium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140730
Marketing Category NameANDA
Application NumberANDA091497
ManufacturerRising Pharmaceuticals, Inc
Substance NameLOSARTAN POTASSIUM
Strength100
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/16571-502-30





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