Package 51655-665-25

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 51655-665-25
Digits Only 5165566525
Product NDC 51655-665
Description

60 TABLET in 1 BOTTLE, PLASTIC (51655-665-25)

Marketing

Marketing Status
Marketed Since 2022-12-16
Brand oxybutynin chloride
Generic oxybutynin chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4950ae3a-d3c8-b948-e063-6394a90afa44", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["f330b7a0-bbe0-0f00-e053-2a95a90a37b8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-665-25)", "package_ndc": "51655-665-25", "marketing_start_date": "20221216"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-665-52)", "package_ndc": "51655-665-52", "marketing_start_date": "20220809"}], "brand_name": "Oxybutynin Chloride", "product_id": "51655-665_4950ae3a-d3c8-b948-e063-6394a90afa44", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "51655-665", "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": "ANDA209823", "marketing_category": "ANDA", "marketing_start_date": "20220809", "listing_expiration_date": "20271231"}