Package 44523-605-16

Brand: sodium sulfacetamide and sulfur

Generic: sodium sulfacetamide, sulfur
NDC Package

Package Facts

Identity

Package NDC 44523-605-16
Digits Only 4452360516
Product NDC 44523-605
Product ID 44523-605_4837c1d3-30b4-4599-e063-6394a90afdbf
Description

454 g in 1 BOTTLE, PLASTIC (44523-605-16)

Marketing

Marketing Status
Marketed Since 2011-04-15
Brand sodium sulfacetamide and sulfur
Generic sodium sulfacetamide, sulfur
Sample Package No

Linked Drug Pages (1)

SODIUM SULFACETAMIDE AND SULFUR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4837c1d3-30b4-4599-e063-6394a90afdbf", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "spl_set_id": ["61e1497d-40ff-0c87-e053-2991aa0a2943"], "manufacturer_name": ["BioComp Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "454 g in 1 BOTTLE, PLASTIC (44523-605-16)", "package_ndc": "44523-605-16", "marketing_start_date": "20110415"}], "brand_name": "SODIUM SULFACETAMIDE AND SULFUR", "product_id": "44523-605_4837c1d3-30b4-4599-e063-6394a90afdbf", "dosage_form": "LOTION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "44523-605", "generic_name": "sodium sulfacetamide, sulfur", "labeler_name": "BioComp Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM SULFACETAMIDE AND SULFUR", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "90 mg/g"}, {"name": "SULFUR", "strength": "45 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20110415", "listing_expiration_date": "20271231"}