Package 68788-8141-9

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 68788-8141-9
Digits Only 6878881419
Product NDC 68788-8141
Product ID 68788-8141_c96411f4-50fe-42a7-9463-5bb9d2939ac3
Description

90 TABLET in 1 BOTTLE, PLASTIC (68788-8141-9)

Marketing

Marketing Status
Marketed Since 2022-02-11
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": "c96411f4-50fe-42a7-9463-5bb9d2939ac3", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["0e002fe8-fa3f-4a7d-84df-0c6e031e6ae4"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (68788-8141-9)", "package_ndc": "68788-8141-9", "marketing_start_date": "20220211"}], "brand_name": "Oxybutynin Chloride", "product_id": "68788-8141_c96411f4-50fe-42a7-9463-5bb9d2939ac3", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "68788-8141", "generic_name": "Oxybutynin Chloride", "labeler_name": "Preferred 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": "20220211", "listing_expiration_date": "20271231"}