Package 59365-5030-0

Brand: trimo san

Generic: oxyquinoline sulfate and sodium lauryl sulfate
NDC Package

Package Facts

Identity

Package NDC 59365-5030-0
Digits Only 5936550300
Product NDC 59365-5030
Product ID 59365-5030_545cdcec-f36b-451d-92be-8a4b21e70719
Description

113.4 g in 1 TUBE (59365-5030-0)

Marketing

Marketing Status
Discontinued 2026-10-31
Brand trimo san
Generic oxyquinoline sulfate and sodium lauryl sulfate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["VAGINAL"], "spl_id": "545cdcec-f36b-451d-92be-8a4b21e70719", "openfda": {"unii": ["61VUG75Y3P", "368GB5141J"], "rxcui": ["999638", "999640"], "spl_set_id": ["1e4a1caa-e6ba-44ef-8347-07e6385a7c9e"], "manufacturer_name": ["CooperSurgical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "113.4 g in 1 TUBE (59365-5030-0)", "package_ndc": "59365-5030-0", "marketing_end_date": "20261031", "marketing_start_date": "19770401"}], "brand_name": "TRIMO SAN", "product_id": "59365-5030_545cdcec-f36b-451d-92be-8a4b21e70719", "dosage_form": "JELLY", "product_ndc": "59365-5030", "generic_name": "Oxyquinoline Sulfate and Sodium Lauryl Sulfate", "labeler_name": "CooperSurgical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRIMO SAN", "active_ingredients": [{"name": "OXYQUINOLINE SULFATE", "strength": ".25 mg/g"}, {"name": "SODIUM LAURYL SULFATE", "strength": ".1 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_end_date": "20261031", "marketing_start_date": "19770401"}