Package 69367-244-10

Brand: sodium sulfacetamide, sulfur

Generic: sulfacetamide sodium and sulfur
NDC Package

Package Facts

Identity

Package NDC 69367-244-10
Digits Only 6936724410
Product NDC 69367-244
Description

285 g in 1 BOTTLE (69367-244-10)

Marketing

Marketing Status
Marketed Since 2020-05-05
Brand sodium sulfacetamide, sulfur
Generic sulfacetamide sodium and sulfur
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4fe0b59c-b850-44db-9670-a7499c724fea", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["1494169"], "spl_set_id": ["4478ac49-8984-42db-9b9e-bea6346a6955"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "285 g in 1 BOTTLE (69367-244-10)", "package_ndc": "69367-244-10", "marketing_start_date": "20200505"}], "brand_name": "SODIUM SULFACETAMIDE, SULFUR", "product_id": "69367-244_4fe0b59c-b850-44db-9670-a7499c724fea", "dosage_form": "LIQUID", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "69367-244", "generic_name": "sulfacetamide sodium and sulfur", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM SULFACETAMIDE, SULFUR", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "98 mg/g"}, {"name": "SULFUR", "strength": "48 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200505", "listing_expiration_date": "20261231"}