Package 72789-049-90

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 72789-049-90
Digits Only 7278904990
Product NDC 72789-049
Product ID 72789-049_4af5faa0-1358-7489-e063-6294a90aae4e
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-049-90)

Marketing

Marketing Status
Marketed Since 2020-01-28
Brand oxybutynin chloride
Generic oxybutynin chloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4af5faa0-1358-7489-e063-6294a90aae4e", "openfda": {"upc": ["0372789049908"], "unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["a1f8be75-2eb9-4eef-8fb4-144ef2bf7ae1"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-049-90)", "package_ndc": "72789-049-90", "marketing_start_date": "20200128"}], "brand_name": "oxybutynin chloride", "product_id": "72789-049_4af5faa0-1358-7489-e063-6294a90aae4e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72789-049", "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": "10 mg/1"}], "application_number": "ANDA207138", "marketing_category": "ANDA", "marketing_start_date": "20161220", "listing_expiration_date": "20271231"}