NDC 64980-679 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC64980-679

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
RISING PHARMA HOLDINGS, INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209025
Marketed since
April 27, 2026
Listing expires
December 31, 2027
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
64980-679-01100 TABLET in 1 BOTTLE (64980-679-01)Jul 18, 2026
64980-679-101000 TABLET in 1 BOTTLE (64980-679-10)Apr 27, 2026
64980-679-50500 TABLET in 1 BOTTLE (64980-679-50)Apr 27, 2026

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