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Oxybutynin Chloride - oxybutynin chloride

Navigation: NDC > Supplier starting with: U > UDL LABORATORIES, INC.
Field Value
NDC Code: 51079-722
Proprietary Name: Oxybutynin Chloride
Suffix:
Non-Proprietary Name: oxybutynin chloride
Dosage Form: TABLET, FILM COATED, EXTENDED RELEASE
Method: ORAL
Original Marketing Date: 14-01-2011
Category Name: ANDA
Application Number: ANDA076702
Labeler: UDL LABORATORIES, INC.
Substance Name: OXYBUTYNIN CHLORIDE
Active Numerator Strength: 5
Active Ingredient Unit: mg/1
Pharm Classes: Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
DEA Schedule: