"64980-209-05" National Drug Code (NDC)

Oxybutynin Chloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-209-05)
(Rising Pharma Holdings, Inc.)

NDC Code64980-209-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-209-05)
Product NDC64980-209
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Proprietary Name SuffixExtended Release
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20160927
Marketing Category NameANDA
Application NumberANDA206121
ManufacturerRising Pharma Holdings, Inc.
Substance NameOXYBUTYNIN CHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

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