"70518-1205-0" National Drug Code (NDC)

Oxybutynin Chloride 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1205-0)
(REMEDYREPACK INC.)

NDC Code70518-1205-0
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1205-0)
Product NDC70518-1205
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180515
Marketing Category NameANDA
Application NumberANDA076702
ManufacturerREMEDYREPACK INC.
Substance NameOXYBUTYNIN CHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

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