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"67296-2335-3" National Drug Code (NDC)

Oxybutynin 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-2335-3)
(Redpharm Drug)

NDC Code67296-2335-3
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-2335-3)
Product NDC67296-2335
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
ManufacturerRedpharm Drug
Substance NameOXYBUTYNIN CHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67296-2335-3





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