"0378-6605-05" National Drug Code (NDC)

Oxybutynin Chloride 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6605-05)
(Mylan Pharmaceuticals Inc.)

NDC Code0378-6605-05
Package Description500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6605-05)
Product NDC0378-6605
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20061110
End Marketing Date20200131
Marketing Category NameANDA
Application NumberANDA076702
ManufacturerMylan Pharmaceuticals Inc.
Substance NameOXYBUTYNIN CHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesCholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

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