Package 72189-130-30

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 72189-130-30
Digits Only 7218913030
Product NDC 72189-130
Product ID 72189-130_2bece08b-b60b-a15e-e063-6394a90a3a13
Description

30 TABLET in 1 BOTTLE (72189-130-30)

Marketing

Marketing Status
Marketed Since 2020-11-11
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-b60b-a15e-e063-6394a90a3a13", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863636", "863664"], "spl_set_id": ["b3d6d2a8-97c4-5bad-e053-2a95a90a155d"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-130-30)", "package_ndc": "72189-130-30", "marketing_start_date": "20201111"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "72189-130_2bece08b-b60b-a15e-e063-6394a90a3a13", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72189-130", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYBUTYNIN CHLORIDE", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA071655", "marketing_category": "ANDA", "marketing_start_date": "20201111", "listing_expiration_date": "20261231"}