Package 67046-1600-3
Brand: oxybutynin chloride
Generic: oxybutynin chloridePackage Facts
Identity
Package NDC
67046-1600-3
Digits Only
6704616003
Product NDC
67046-1600
Description
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1600-3)
Marketing
Marketing Status
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": "46b2b02c-85d8-8404-e063-6294a90a0eef", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863628"], "spl_set_id": ["3f7dc283-b168-8251-e063-6294a90a45a2"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1600-3)", "package_ndc": "67046-1600-3", "marketing_start_date": "20250923"}], "brand_name": "Oxybutynin Chloride", "product_id": "67046-1600_46b2b02c-85d8-8404-e063-6294a90a0eef", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "67046-1600", "generic_name": "Oxybutynin Chloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA211655", "marketing_category": "ANDA", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}