Package 81542-202-12

Brand: sulfacetamide sodium, sulfur

Generic: sulfacetamide sodium, sulfur
NDC Package

Package Facts

Identity

Package NDC 81542-202-12
Digits Only 8154220212
Product NDC 81542-202
Product ID 81542-202_36c18a52-2828-aaa0-e063-6294a90a6ce1
Description

355 mL in 1 BOTTLE (81542-202-12)

Marketing

Marketing Status
Marketed Since 2023-02-08
Brand sulfacetamide sodium, sulfur
Generic sulfacetamide sodium, sulfur
Sample Package No

Linked Drug Pages (1)

SULFACETAMIDE SODIUM, SULFUR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "36c18a52-2828-aaa0-e063-6294a90a6ce1", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["999613"], "spl_set_id": ["f433db67-d8a6-320e-e053-2995a90aab52"], "manufacturer_name": ["Bantry Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (81542-202-12)", "package_ndc": "81542-202-12", "marketing_start_date": "20230208"}], "brand_name": "SULFACETAMIDE SODIUM, SULFUR", "product_id": "81542-202_36c18a52-2828-aaa0-e063-6294a90a6ce1", "dosage_form": "SOLUTION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "81542-202", "generic_name": "SULFACETAMIDE SODIUM, SULFUR", "labeler_name": "Bantry Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SULFACETAMIDE SODIUM, SULFUR", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}, {"name": "SULFUR", "strength": "50 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20230208", "listing_expiration_date": "20261231"}