NDC 70771-1086 – Oxybutynin

Oxybutynin Chloride 5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC70771-1086

Product details

Brand name
Oxybutynin
Generic name
Oxybutynin
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202332
Marketed since
August 10, 2017
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Oxybutynin →

Package NDC codes (6)

Package NDCDescriptionSince
70771-1086-1100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-1)Aug 10, 2017
70771-1086-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-3)Aug 10, 2017
70771-1086-410 BLISTER PACK in 1 CARTON (70771-1086-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1086-2)Aug 10, 2017
70771-1086-5500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-5)Aug 10, 2017
70771-1086-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-6)Aug 10, 2017
70771-1086-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-9)Aug 10, 2017

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