Package 72189-132-30

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 72189-132-30
Digits Only 7218913230
Product NDC 72189-132
Product ID 72189-132_2bece08b-b60c-a15e-e063-6394a90a3a13
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)

Marketing

Marketing Status
Marketed Since 2020-08-24
Brand oxybutynin chloride
Generic oxybutynin chloride
Sample Package No

Linked Drug Pages (1)

OXYBUTYNIN CHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2bece08b-b60c-a15e-e063-6394a90a3a13", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["ada3be87-2cdd-75f7-e053-2995a90aa95b"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)", "package_ndc": "72189-132-30", "marketing_start_date": "20200824"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "72189-132_2bece08b-b60c-a15e-e063-6394a90a3a13", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72189-132", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "DIRECT RX", "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": "20200824", "listing_expiration_date": "20261231"}