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"51079-722-63" National Drug Code (NDC)

Oxybutynin Chloride 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 DOSE PACK (51079-722-63)
(UDL Laboratories, Inc.)

NDC Code51079-722-63
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 DOSE PACK (51079-722-63)
Product NDC51079-722
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20110114
Marketing Category NameANDA
Application NumberANDA076702
ManufacturerUDL Laboratories, Inc.
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/51079-722-63





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