Package 42291-914-50

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 42291-914-50
Digits Only 4229191450
Product NDC 42291-914
Description

500 TABLET in 1 BOTTLE (42291-914-50)

Marketing

Marketing Status
Marketed Since 2022-09-30
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": "48bf6717-5f99-d204-e063-6294a90af39d", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["e9e61a32-d815-2fa3-e053-2a95a90a63ee"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (42291-914-50)", "package_ndc": "42291-914-50", "marketing_start_date": "20220930"}], "brand_name": "Oxybutynin Chloride", "product_id": "42291-914_48bf6717-5f99-d204-e063-6294a90af39d", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "42291-914", "generic_name": "oxybutynin chloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA075079", "marketing_category": "ANDA", "marketing_start_date": "20220930", "listing_expiration_date": "20271231"}