sulfacetamide sodium
Generic: sulfacetamide sodium
Labeler: bausch & lomb incorporatedDrug Facts
Product Profile
Brand Name
sulfacetamide sodium
Generic Name
sulfacetamide sodium
Labeler
bausch & lomb incorporated
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
sulfacetamide sodium 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24208-670
Product ID
24208-670_39869c1b-2b30-482e-b88e-9177cd85ea16
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040066
Listing Expiration
2026-12-31
Marketing Start
1994-12-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24208670
Hyphenated Format
24208-670
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sulfacetamide sodium (source: ndc)
Generic Name
sulfacetamide sodium (source: ndc)
Application Number
ANDA040066 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (24208-670-04) / 15 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
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"}