Package 67296-2045-3

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 67296-2045-3
Digits Only 6729620453
Product NDC 67296-2045
Product ID 67296-2045_2c6318c6-0896-4b52-e063-6394a90a4e53
Description

30 TABLET in 1 BOTTLE (67296-2045-3)

Marketing

Marketing Status
Marketed Since 2019-11-01
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": "2c6318c6-0896-4b52-e063-6394a90a4e53", "openfda": {"upc": ["0369315182109", "0369315182055", "0369315182017"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["fc4cfbe6-a940-41c0-e053-6294a90adb14"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2045-3)", "package_ndc": "67296-2045-3", "marketing_start_date": "20191101"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "67296-2045_2c6318c6-0896-4b52-e063-6394a90a4e53", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "67296-2045", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYBUTYNIN CHLORIDE", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA212798", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}