Package 44523-613-06

Brand: sodium sulfacetamide

Generic: sodium sulfacetamide
NDC Package

Package Facts

Identity

Package NDC 44523-613-06
Digits Only 4452361306
Product NDC 44523-613
Description

177 mL in 1 BOTTLE, PLASTIC (44523-613-06)

Marketing

Marketing Status
Marketed Since 2011-09-07
Brand sodium sulfacetamide
Generic sodium sulfacetamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4839e157-d35d-c2f2-e063-6394a90ae389", "openfda": {"unii": ["4NRT660KJQ"], "rxcui": ["1006107"], "spl_set_id": ["efde52a6-216d-4ccc-8574-5e3e41ec7e06"], "manufacturer_name": ["BioComp Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (44523-613-06)", "package_ndc": "44523-613-06", "marketing_start_date": "20110907"}], "brand_name": "SODIUM SULFACETAMIDE", "product_id": "44523-613_4839e157-d35d-c2f2-e063-6394a90ae389", "dosage_form": "LIQUID", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "44523-613", "generic_name": "SODIUM SULFACETAMIDE", "labeler_name": "BioComp Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM SULFACETAMIDE", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20110907", "listing_expiration_date": "20271231"}