Package 45802-896-26

Brand: sulfacetamide sodium

Generic: sulfacetamide sodium
NDC Package

Package Facts

Identity

Package NDC 45802-896-26
Digits Only 4580289626
Product NDC 45802-896
Description

118 mL in 1 BOTTLE, PLASTIC (45802-896-26)

Marketing

Marketing Status
Marketed Since 2012-10-17
Brand sulfacetamide sodium
Generic sulfacetamide sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "03f16a28-7c10-4fa0-a4c8-ac29335c6be7", "openfda": {"unii": ["4NRT660KJQ"], "rxcui": ["1006688"], "spl_set_id": ["4fb4d39a-330e-4c84-abbc-3b33b36b206f"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, PLASTIC (45802-896-26)", "package_ndc": "45802-896-26", "marketing_start_date": "20121017"}], "brand_name": "Sulfacetamide Sodium", "product_id": "45802-896_03f16a28-7c10-4fa0-a4c8-ac29335c6be7", "dosage_form": "LOTION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "45802-896", "generic_name": "Sulfacetamide Sodium", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sulfacetamide Sodium", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}], "application_number": "ANDA078649", "marketing_category": "ANDA", "marketing_start_date": "20121017", "listing_expiration_date": "20261231"}