Package 42192-133-16
Brand: sodium sulfacetamide and sulfur
Generic: sodium sulfacetamide and sulfurPackage Facts
Identity
Package NDC
42192-133-16
Digits Only
4219213316
Product NDC
42192-133
Description
473 mL in 1 BOTTLE (42192-133-16)
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": "888fce7d-dc47-4d1b-9c39-9dfcaa051607", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["1010234"], "spl_set_id": ["c3ff4716-6009-4e29-9da9-ea740726cc3c"], "manufacturer_name": ["Acella Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (42192-133-16)", "package_ndc": "42192-133-16", "marketing_start_date": "20110513"}], "brand_name": "Sodium Sulfacetamide and Sulfur", "product_id": "42192-133_888fce7d-dc47-4d1b-9c39-9dfcaa051607", "dosage_form": "SOLUTION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "42192-133", "generic_name": "Sodium Sulfacetamide and Sulfur", "labeler_name": "Acella 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": "20110513", "listing_expiration_date": "20261231"}