"70771-1088-4" National Drug Code (NDC)

Oxybutynin 10 BLISTER PACK in 1 CARTON (70771-1088-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1088-2)
(Zydus Lifesciences Limited)

NDC Code70771-1088-4
Package Description10 BLISTER PACK in 1 CARTON (70771-1088-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1088-2)
Product NDC70771-1088
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin
Non-Proprietary NameOxybutynin
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20170810
Marketing Category NameANDA
Application NumberANDA202332
ManufacturerZydus Lifesciences Limited
Substance NameOXYBUTYNIN CHLORIDE
Strength15
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

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