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"71205-667-90" National Drug Code (NDC)

Oxybutynin Chloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)
(Proficient Rx LP)

NDC Code71205-667-90
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)
Product NDC71205-667
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxybutynin Chloride
Non-Proprietary NameOxybutynin Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20161220
Marketing Category NameANDA
Application NumberANDA207138
ManufacturerProficient Rx LP
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/71205-667-90





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