Package 50090-6673-0
Brand: oxybutynin chloride extended release
Generic: oxybutynin chloridePackage Facts
Identity
Package NDC
50090-6673-0
Digits Only
5009066730
Product NDC
50090-6673
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6673-0)
Marketing
Marketing Status
Brand
oxybutynin chloride extended release
Generic
oxybutynin chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "92090e0c-c4f0-420d-b3cf-cf54fcf219ff", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["3688227b-7655-40ca-b34b-073a39fd60f4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6673-0)", "package_ndc": "50090-6673-0", "marketing_start_date": "20230901"}], "brand_name": "Oxybutynin Chloride Extended Release", "product_id": "50090-6673_92090e0c-c4f0-420d-b3cf-cf54fcf219ff", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-6673", "generic_name": "Oxybutynin Chloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA206121", "marketing_category": "ANDA", "marketing_start_date": "20160927", "listing_expiration_date": "20271231"}