Package 0615-8219-39

Brand: oxybutynin

Generic: oxybutynin
NDC Package

Package Facts

Identity

Package NDC 0615-8219-39
Digits Only 0615821939
Product NDC 0615-8219
Product ID 0615-8219_7a51ea21-3f85-4693-8e7e-ed031f257496
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8219-39)

Marketing

Marketing Status
Marketed Since 2019-01-25
Brand oxybutynin
Generic oxybutynin
Sample Package No

Linked Drug Pages (1)

oxybutynin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7a51ea21-3f85-4693-8e7e-ed031f257496", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863636"], "spl_set_id": ["ed10f0c9-23d6-4ded-b17f-ed474632a965"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8219-39)", "package_ndc": "0615-8219-39", "marketing_start_date": "20190125"}], "brand_name": "oxybutynin", "product_id": "0615-8219_7a51ea21-3f85-4693-8e7e-ed031f257496", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "0615-8219", "generic_name": "oxybutynin", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxybutynin", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202332", "marketing_category": "ANDA", "marketing_start_date": "20170810", "listing_expiration_date": "20261231"}