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"0093-5207-01" National Drug Code (NDC)

Oxybutynin Chloride 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0093-5207-01)
(TEVA Pharmaceuticals USA Inc)

NDC Code0093-5207-01
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0093-5207-01)
Product NDC0093-5207
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20070511
End Marketing Date20200831
Marketing Category NameANDA
Application NumberANDA076745
ManufacturerTEVA Pharmaceuticals USA Inc
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/0093-5207-01





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