"71930-051-52" National Drug Code (NDC)

Oxybutynin Chloride 500 TABLET in 1 BOTTLE (71930-051-52)
(Eywa Pharma Inc)

NDC Code71930-051-52
Package Description500 TABLET in 1 BOTTLE (71930-051-52)
Product NDC71930-051
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20190715
Marketing Category NameANDA
Application NumberANDA211062
ManufacturerEywa Pharma Inc
Substance NameOXYBUTYNIN CHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

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