NDCFind

Oxybutynin 70771-1086-05

Package NDC

70771-1086-05

Product NDC: 70771-1086

Manufacturer
Zydus Lifesciences Limited
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
August 10, 2017
Listing Expires
December 31, 2026
Application
ANDA202332
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Active Ingredients

IngredientStrength
Oxybutynin Chloride5 mg/1

Drug Class

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

Selected Package

70771-1086-05Selected

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-5)

Other packages for this product(5)

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-1)

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-3)

10 BLISTER PACK in 1 CARTON (70771-1086-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1086-2)

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-6)

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-9)