"70518-0965-0" National Drug Code (NDC)

Oxybutynin Chloride 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0965-0)
(REMEDYREPACK INC.)

NDC Code70518-0965-0
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0965-0)
Product NDC70518-0965
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180118
Marketing Category NameANDA
Application NumberANDA076644
ManufacturerREMEDYREPACK INC.
Substance NameOXYBUTYNIN CHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

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