Package 72789-414-90
Brand: oxybutynin chloride extended release
Generic: oxybutynin chloridePackage Facts
Identity
Package NDC
72789-414-90
Digits Only
7278941490
Product NDC
72789-414
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-414-90)
Marketing
Marketing Status
Brand
oxybutynin chloride extended release
Generic
oxybutynin chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "402fe5d4-f54c-5b91-e063-6294a90a3908", "openfda": {"upc": ["0372789414904"], "unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["e466d963-469a-4b1c-87f9-2e3e1e9bdf3d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-414-90)", "package_ndc": "72789-414-90", "marketing_start_date": "20240611"}], "brand_name": "Oxybutynin Chloride Extended Release", "product_id": "72789-414_402fe5d4-f54c-5b91-e063-6294a90a3908", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72789-414", "generic_name": "Oxybutynin Chloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA206121", "marketing_category": "ANDA", "marketing_start_date": "20160927", "listing_expiration_date": "20261231"}