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"71335-2121-1" National Drug Code (NDC)

Oxybutynin Chloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-1)
(Bryant Ranch Prepack)

NDC Code71335-2121-1
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-1)
Product NDC71335-2121
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
ManufacturerBryant Ranch Prepack
Substance NameOXYBUTYNIN CHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2121-1





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