"72189-132-30" National Drug Code (NDC)

Oxybutynin Chloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)
(DIRECT RX)

NDC Code72189-132-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)
Product NDC72189-132
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200824
Marketing Category NameANDA
Application NumberANDA207138
ManufacturerDIRECT RX
Substance NameOXYBUTYNIN CHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

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