Package 24208-670-04
Brand: sulfacetamide sodium
Generic: sulfacetamide sodiumPackage Facts
Identity
Package NDC
24208-670-04
Digits Only
2420867004
Product NDC
24208-670
Description
1 BOTTLE, DROPPER in 1 CARTON (24208-670-04) / 15 mL in 1 BOTTLE, DROPPER
Marketing
Marketing Status
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": "39869c1b-2b30-482e-b88e-9177cd85ea16", "openfda": {"unii": ["4NRT660KJQ"], "rxcui": ["1006120"], "spl_set_id": ["6c1b2658-e756-4f31-9bc8-f99a0baa4637"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-670-04) / 15 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-670-04", "marketing_start_date": "19941228"}], "brand_name": "Sulfacetamide Sodium", "product_id": "24208-670_39869c1b-2b30-482e-b88e-9177cd85ea16", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "24208-670", "generic_name": "sulfacetamide sodium", "labeler_name": "Bausch & Lomb Incorporated", "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"}