Package 71335-2940-1

Brand: sodium sulfacetamide and sulfur

Generic: sulfacetamide sodium, sulfur
NDC Package

Package Facts

Identity

Package NDC 71335-2940-1
Digits Only 7133529401
Product NDC 71335-2940
Description

227 g in 1 BOTTLE, PLASTIC (71335-2940-1)

Marketing

Marketing Status
Marketed Since 2025-10-29
Brand sodium sulfacetamide and 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": "42535bb6-59d5-38d1-e063-6294a90a7754", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["999613"], "spl_set_id": ["2a8c6cc3-62b6-4682-9670-df9c0e6cb2e1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 BOTTLE, PLASTIC (71335-2940-1)", "package_ndc": "71335-2940-1", "marketing_start_date": "20251029"}], "brand_name": "Sodium Sulfacetamide and Sulfur", "product_id": "71335-2940_42535bb6-59d5-38d1-e063-6294a90a7754", "dosage_form": "LIQUID", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "71335-2940", "generic_name": "SULFACETAMIDE SODIUM, SULFUR", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Sulfacetamide and Sulfur", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/g"}, {"name": "SULFUR", "strength": "50 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20211115", "listing_expiration_date": "20261231"}