Package 69367-245-16
Brand: sodium sulfacetamide and sulfur
Generic: sodium sulfacetamide and sulfurPackage Facts
Identity
Package NDC
69367-245-16
Digits Only
6936724516
Product NDC
69367-245
Description
473 mL in 1 BOTTLE (69367-245-16)
Marketing
Marketing Status
Brand
sodium sulfacetamide and sulfur
Generic
sodium sulfacetamide and sulfur
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "b4e89e57-397a-4578-bc59-709cb46db033", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["1010234"], "spl_set_id": ["e9b60d3f-3f3f-477d-92d7-fe0ba07e21de"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (69367-245-16)", "package_ndc": "69367-245-16", "marketing_start_date": "20210618"}], "brand_name": "Sodium Sulfacetamide and Sulfur", "product_id": "69367-245_b4e89e57-397a-4578-bc59-709cb46db033", "dosage_form": "SUSPENSION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "69367-245", "generic_name": "Sodium Sulfacetamide and Sulfur", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Sulfacetamide and Sulfur", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "80 mg/mL"}, {"name": "SULFUR", "strength": "40 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210618", "listing_expiration_date": "20261231"}