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"0603-3739-32" National Drug Code (NDC)

Furosemide 1000 TABLET in 1 BOTTLE, PLASTIC (0603-3739-32)
(Qualitest Pharmaceuticals)

NDC Code0603-3739-32
Package Description1000 TABLET in 1 BOTTLE, PLASTIC (0603-3739-32)
Product NDC0603-3739
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFurosemide
Non-Proprietary NameFurosemide
Dosage FormTABLET
UsageORAL
Start Marketing Date20040326
End Marketing Date20180930
Marketing Category NameANDA
Application NumberANDA076796
ManufacturerQualitest Pharmaceuticals
Substance NameFUROSEMIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0603-3739-32





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