NDCFind

Oxybutynin Chloride 69315-0182

Product NDC

69315-0182
Manufacturer
Leading Pharma, Llc
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
November 1, 2019
Listing Expires
December 31, 2026
Application
ANDA212798
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Active Ingredients

IngredientStrength
Oxybutynin Chloride5 mg/1

Drug Class

Cholinergic Muscarinic Antagonist [EPC]Cholinergic Muscarinic Antagonists [MoA]

Packaging Options(3)

100 TABLET in 1 BOTTLE (69315-182-01)

500 TABLET in 1 BOTTLE (69315-182-05)

1000 TABLET in 1 BOTTLE (69315-182-10)