Package 73352-750-01

Brand: sodium sulfacetamide and sulfer emulsion

Generic: sodium sulfacetamide and sulfer
NDC Package

Package Facts

Identity

Package NDC 73352-750-01
Digits Only 7335275001
Product NDC 73352-750
Description

177 mL in 1 BOTTLE (73352-750-01)

Marketing

Marketing Status
Marketed Since 2025-10-04
Brand sodium sulfacetamide and sulfer emulsion
Generic sodium sulfacetamide and sulfer
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "41396a22-cc34-94f2-e063-6294a90afb65", "openfda": {"upc": ["0373352750016"], "unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["999604"], "spl_set_id": ["40601d03-aea0-b0a6-e063-6394a90a1698"], "manufacturer_name": ["Trifluent Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE (73352-750-01)", "package_ndc": "73352-750-01", "marketing_start_date": "20251004"}], "brand_name": "Sodium Sulfacetamide and Sulfer Emulsion", "product_id": "73352-750_41396a22-cc34-94f2-e063-6294a90afb65", "dosage_form": "EMULSION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "73352-750", "generic_name": "Sodium Sulfacetamide and Sulfer", "labeler_name": "Trifluent Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Sulfacetamide and Sulfer Emulsion", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}, {"name": "SULFUR", "strength": "10 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20251004", "listing_expiration_date": "20261231"}