Package 50090-7766-0

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 50090-7766-0
Digits Only 5009077660
Product NDC 50090-7766
Description

90 TABLET in 1 BOTTLE (50090-7766-0)

Marketing

Marketing Status
Marketed Since 2025-11-12
Brand oxybutynin chloride
Generic oxybutynin chloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "495472e9-88f2-4df2-b2e9-f3c5b5806cd9", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["44990ed6-b8e7-40f5-b636-e848024ec6d8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7766-0)", "package_ndc": "50090-7766-0", "marketing_start_date": "20251112"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "50090-7766_495472e9-88f2-4df2-b2e9-f3c5b5806cd9", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-7766", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYBUTYNIN CHLORIDE", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209025", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}