Package 50090-5353-0

Brand: oxybutynin

Generic: oxybutynin
NDC Package

Package Facts

Identity

Package NDC 50090-5353-0
Digits Only 5009053530
Product NDC 50090-5353
Product ID 50090-5353_2d660e74-e22d-4493-9e7b-51c8031c3c69
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5353-0)

Marketing

Marketing Status
Marketed Since 2020-11-11
Brand oxybutynin
Generic oxybutynin
Sample Package No

Linked Drug Pages (1)

oxybutynin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d660e74-e22d-4493-9e7b-51c8031c3c69", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["1f95920c-5dc2-44e4-b61d-b2c5e05390ba"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5353-0)", "package_ndc": "50090-5353-0", "marketing_start_date": "20201111"}], "brand_name": "oxybutynin", "product_id": "50090-5353_2d660e74-e22d-4493-9e7b-51c8031c3c69", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-5353", "generic_name": "oxybutynin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxybutynin", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202332", "marketing_category": "ANDA", "marketing_start_date": "20170810", "listing_expiration_date": "20261231"}