Package 72789-490-60

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 72789-490-60
Digits Only 7278949060
Product NDC 72789-490
Product ID 72789-490_2f24ff93-475c-5845-e063-6394a90a8faa
Description

60 TABLET in 1 BOTTLE, PLASTIC (72789-490-60)

Marketing

Marketing Status
Marketed Since 2025-02-27
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": "2f24ff93-475c-5845-e063-6394a90a8faa", "openfda": {"upc": ["0372789490601"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["3a319017-4e25-402e-8ba0-63b9f1eb707e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-490-60)", "package_ndc": "72789-490-60", "marketing_start_date": "20250227"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "72789-490_2f24ff93-475c-5845-e063-6394a90a8faa", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72789-490", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}