Package 82804-095-30

Brand: oxybutynin chloride extended release

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 82804-095-30
Digits Only 8280409530
Product NDC 82804-095
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-095-30)

Marketing

Marketing Status
Marketed Since 2024-04-02
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": "7d2332b4-9e48-4bb2-a2c3-75e16e1d455b", "openfda": {"upc": ["0382804095308"], "unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["7d2332b4-9e48-4bb2-a2c3-75e16e1d455b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-095-30)", "package_ndc": "82804-095-30", "marketing_start_date": "20240402"}], "brand_name": "Oxybutynin Chloride Extended Release", "product_id": "82804-095_7d2332b4-9e48-4bb2-a2c3-75e16e1d455b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "82804-095", "generic_name": "Oxybutynin Chloride", "labeler_name": "Proficient Rx LP", "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"}