Package 43063-931-30

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 43063-931-30
Digits Only 4306393130
Product NDC 43063-931
Description

30 TABLET in 1 BOTTLE, PLASTIC (43063-931-30)

Marketing

Marketing Status
Marketed Since 2019-01-09
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": "302c054b-7dcb-1396-e063-6394a90ac66e", "openfda": {"upc": ["0343063931301"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["9c8ced4b-94de-4df8-bea3-b42b8846b769"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-931-30)", "package_ndc": "43063-931-30", "marketing_start_date": "20190109"}], "brand_name": "Oxybutynin Chloride", "product_id": "43063-931_302c054b-7dcb-1396-e063-6394a90ac66e", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "43063-931", "generic_name": "Oxybutynin Chloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209335", "marketing_category": "ANDA", "marketing_start_date": "20171222", "listing_expiration_date": "20261231"}