Package 44523-550-08

Brand: sodium sulfacetamide, sulfur

Generic: sulfacetamide sodium, sulfur
NDC Package

Package Facts

Identity

Package NDC 44523-550-08
Digits Only 4452355008
Product NDC 44523-550
Description

227 g in 1 BOTTLE, PLASTIC (44523-550-08)

Marketing

Marketing Status
Marketed Since 2011-09-15
Brand sodium sulfacetamide, sulfur
Generic sulfacetamide sodium, sulfur
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "f798f8d7-639f-2a12-e053-6294a90a00fb", "openfda": {"upc": ["0344523550087"], "unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["1000895"], "spl_set_id": ["99e52390-478e-49ed-87de-aa794379bfeb"], "manufacturer_name": ["BioComp Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 BOTTLE, PLASTIC (44523-550-08)", "package_ndc": "44523-550-08", "marketing_start_date": "20110915"}], "brand_name": "Sodium Sulfacetamide, Sulfur", "product_id": "44523-550_f798f8d7-639f-2a12-e053-6294a90a00fb", "dosage_form": "EMULSION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "44523-550", "generic_name": "SULFACETAMIDE SODIUM, SULFUR", "labeler_name": "BioComp Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Sulfacetamide, Sulfur", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/g"}, {"name": "SULFUR", "strength": "20 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20110915", "listing_expiration_date": "20261231"}