NDC 64980-211 – Oxybutynin Chloride Extended Release

Oxybutynin Chloride 15 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC64980-211

Product details

Brand name
Oxybutynin Chloride Extended Release
Generic name
Oxybutynin Chloride
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206121
Marketed since
September 27, 2016
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
64980-211-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-211-01)Sep 27, 2016
64980-211-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-211-05)Mar 29, 2022

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