Package 82868-047-30

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 82868-047-30
Digits Only 8286804730
Product NDC 82868-047
Product ID 82868-047_46dcbc0b-febf-ab63-e063-6394a90aee4c
Description

30 TABLET in 1 BOTTLE, PLASTIC (82868-047-30)

Marketing

Marketing Status
Marketed Since 2024-02-19
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": "46dcbc0b-febf-ab63-e063-6394a90aee4c", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["13a79659-a181-6a61-e063-6294a90ae034"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-047-30)", "package_ndc": "82868-047-30", "marketing_start_date": "20240219"}], "brand_name": "Oxybutynin Chloride", "product_id": "82868-047_46dcbc0b-febf-ab63-e063-6394a90aee4c", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "82868-047", "generic_name": "Oxybutynin Chloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209335", "marketing_category": "ANDA", "marketing_start_date": "20240219", "listing_expiration_date": "20261231"}