NDC 0615-8492 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0615-8492

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212798
Marketed since
November 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Oxybutynin Chloride →

Package NDC codes (2)

Package NDCDescriptionSince
0615-8492-0515 TABLET in 1 BLISTER PACK (0615-8492-05)Oct 3, 2023
0615-8492-3930 TABLET in 1 BLISTER PACK (0615-8492-39)Oct 3, 2023

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