Package 71205-667-90

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 71205-667-90
Digits Only 7120566790
Product NDC 71205-667
Product ID 71205-667_88f08450-559e-4038-aad1-051e4ab283cf
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)

Marketing

Marketing Status
Marketed Since 2022-06-08
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": "88f08450-559e-4038-aad1-051e4ab283cf", "openfda": {"upc": ["0371205667306"], "unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["88f08450-559e-4038-aad1-051e4ab283cf"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-30)", "package_ndc": "71205-667-30", "marketing_start_date": "20220608"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-60)", "package_ndc": "71205-667-60", "marketing_start_date": "20220608"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)", "package_ndc": "71205-667-90", "marketing_start_date": "20220608"}], "brand_name": "oxybutynin chloride", "product_id": "71205-667_88f08450-559e-4038-aad1-051e4ab283cf", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "71205-667", "generic_name": "oxybutynin chloride", "labeler_name": "Proficient Rx LP", "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": "20161220", "listing_expiration_date": "20261231"}