Package 67046-1599-3

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 67046-1599-3
Digits Only 6704615993
Product NDC 67046-1599
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1599-3)

Marketing

Marketing Status
Marketed Since 2025-09-23
Brand oxybutynin chloride
Generic oxybutynin chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46b2b040-89e8-d5ff-e063-6394a90a18c1", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863636"], "spl_set_id": ["3f7da2a3-ca46-d3e8-e063-6294a90abef3"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1599-3)", "package_ndc": "67046-1599-3", "marketing_start_date": "20250923"}], "brand_name": "Oxybutynin Chloride", "product_id": "67046-1599_46b2b040-89e8-d5ff-e063-6394a90a18c1", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "67046-1599", "generic_name": "Oxybutynin Chloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211655", "marketing_category": "ANDA", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}