NDC 70954-005 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70954-005

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209823
Marketed since
November 15, 2017
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
70954-005-10100 TABLET in 1 BOTTLE (70954-005-10)Nov 15, 2017
70954-005-20500 TABLET in 1 BOTTLE (70954-005-20)Nov 15, 2017
70954-005-301000 TABLET in 1 BOTTLE (70954-005-30)Nov 15, 2017
70954-005-50100 BLISTER PACK in 1 CARTON (70954-005-50) / 1 TABLET in 1 BLISTER PACK (70954-005-40)Aug 20, 2021

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