Package 50090-4307-0

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 50090-4307-0
Digits Only 5009043070
Product NDC 50090-4307
Product ID 50090-4307_9e1b91d5-d9c0-4b55-b5d5-048879327725
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4307-0)

Marketing

Marketing Status
Marketed Since 2019-05-23
Brand oxybutynin chloride
Generic oxybutynin chloride
Sample Package No

Linked Drug Pages (1)

oxybutynin chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9e1b91d5-d9c0-4b55-b5d5-048879327725", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["8f147f73-cfc6-40a3-b1a3-e4cab1868523"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4307-0)", "package_ndc": "50090-4307-0", "marketing_start_date": "20190523"}], "brand_name": "oxybutynin chloride", "product_id": "50090-4307_9e1b91d5-d9c0-4b55-b5d5-048879327725", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-4307", "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": "10 mg/1"}], "application_number": "ANDA207138", "marketing_category": "ANDA", "marketing_start_date": "20161220", "listing_expiration_date": "20261231"}