Package 76420-090-15

Brand: sulfacetamide sodium

Generic: sulfacetamide sodium
NDC Package

Package Facts

Identity

Package NDC 76420-090-15
Digits Only 7642009015
Product NDC 76420-090
Description

15 mL in 1 BOTTLE, DROPPER (76420-090-15)

Marketing

Marketing Status
Marketed Since 2020-10-24
Brand sulfacetamide sodium
Generic sulfacetamide sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "b26a1d2a-bf50-4787-e053-2a95a90a951b", "openfda": {"unii": ["4NRT660KJQ"], "rxcui": ["1006120"], "spl_set_id": ["129d5dd9-32a4-4398-862d-820cd4468448"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE, DROPPER (76420-090-15)", "package_ndc": "76420-090-15", "marketing_start_date": "20201024"}], "brand_name": "Sulfacetamide Sodium", "product_id": "76420-090_b26a1d2a-bf50-4787-e053-2a95a90a951b", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "76420-090", "generic_name": "sulfacetamide sodium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sulfacetamide Sodium", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}], "application_number": "ANDA040066", "marketing_category": "ANDA", "marketing_start_date": "19941228", "listing_expiration_date": "20261231"}