"69452-121-20" National Drug Code (NDC)

Oxybutynin Chloride 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69452-121-20)
(Bionpharma Inc.)

NDC Code69452-121-20
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69452-121-20)
Product NDC69452-121
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200316
Marketing Category NameANDA
Application NumberANDA210717
ManufacturerBionpharma Inc.
Substance NameOXYBUTYNIN CHLORIDE
Strength15
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

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