Package 42192-139-01

Brand: sodium sulfacetamide, sulfur

Generic: sodium sulfacetamide and sulfur
NDC Package

Package Facts

Identity

Package NDC 42192-139-01
Digits Only 4219213901
Product NDC 42192-139
Product ID 42192-139_db2b5db3-6b73-4292-874e-d1893b647429
Description

28 g in 1 TUBE (42192-139-01)

Marketing

Marketing Status
Marketed Since 2014-06-11
Brand sodium sulfacetamide, sulfur
Generic sodium sulfacetamide and sulfur
Sample Package No

Linked Drug Pages (1)

SODIUM SULFACETAMIDE, SULFUR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "db2b5db3-6b73-4292-874e-d1893b647429", "openfda": {"unii": ["70FD1KFU70", "4NRT660KJQ"], "rxcui": ["1005834"], "spl_set_id": ["99705c54-b7af-423d-8f20-881e8fea236f"], "manufacturer_name": ["Acella Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28 g in 1 TUBE (42192-139-01)", "package_ndc": "42192-139-01", "marketing_start_date": "20140611"}], "brand_name": "SODIUM SULFACETAMIDE, SULFUR", "product_id": "42192-139_db2b5db3-6b73-4292-874e-d1893b647429", "dosage_form": "CREAM", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "42192-139", "generic_name": "Sodium Sulfacetamide and Sulfur", "labeler_name": "Acella Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM SULFACETAMIDE, SULFUR", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/g"}, {"name": "SULFUR", "strength": "50 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}