Package 42192-146-12

Brand: sodium sulfacetamide

Generic: sodium sulfacetamide
NDC Package

Package Facts

Identity

Package NDC 42192-146-12
Digits Only 4219214612
Product NDC 42192-146
Product ID 42192-146_3e60a6f5-e598-1049-e063-6394a90acddd
Description

355 mL in 1 BOTTLE (42192-146-12)

Marketing

Marketing Status
Discontinued 2026-05-09
Brand sodium sulfacetamide
Generic sodium sulfacetamide
Sample Package No

Linked Drug Pages (1)

Sodium Sulfacetamide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3e60a6f5-e598-1049-e063-6394a90acddd", "openfda": {"unii": ["4NRT660KJQ"], "rxcui": ["1006107"], "spl_set_id": ["c7b051aa-a1c4-4f0e-9278-2387155857b0"], "manufacturer_name": ["Acella Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (42192-146-12)", "package_ndc": "42192-146-12", "marketing_end_date": "20260509", "marketing_start_date": "20141010"}], "brand_name": "Sodium Sulfacetamide", "product_id": "42192-146_3e60a6f5-e598-1049-e063-6394a90acddd", "dosage_form": "GEL", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "42192-146", "generic_name": "Sodium Sulfacetamide", "labeler_name": "Acella Pharmaceuticals, LLC", "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_end_date": "20260509", "marketing_start_date": "20141010"}