Package 66267-642-30

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 66267-642-30
Digits Only 6626764230
Product NDC 66267-642
Product ID 66267-642_1fa711ca-cee8-fae5-e063-6294a90aa5d0
Description

30 TABLET in 1 BOTTLE (66267-642-30)

Marketing

Marketing Status
Marketed Since 2019-07-25
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": "1fa711ca-cee8-fae5-e063-6294a90aa5d0", "openfda": {"upc": ["0366267642309"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["8e830697-a6d3-13ed-e053-2995a90acb11"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (66267-642-30)", "package_ndc": "66267-642-30", "marketing_start_date": "20190725"}], "brand_name": "Oxybutynin Chloride", "product_id": "66267-642_1fa711ca-cee8-fae5-e063-6294a90aa5d0", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "66267-642", "generic_name": "Oxybutynin Chloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209823", "marketing_category": "ANDA", "marketing_start_date": "20171115", "listing_expiration_date": "20261231"}