sulfacetamide sodium
Generic: sulfacetamide sodium
Labeler: preferred pharmaceuticals, incDrug Facts
Product Profile
Brand Name
sulfacetamide sodium
Generic Name
sulfacetamide sodium
Labeler
preferred pharmaceuticals, inc
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
sulfacetamide sodium 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-9871
Product ID
68788-9871_fe2e1b1d-4502-43a2-90f5-7b06d074ac1b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040066
Listing Expiration
2026-12-31
Marketing Start
2012-02-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687889871
Hyphenated Format
68788-9871
Supplemental Identifiers
RxCUI
UNII
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
- 15 mL in 1 BOTTLE, DROPPER (68788-9871-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "fe2e1b1d-4502-43a2-90f5-7b06d074ac1b", "openfda": {"unii": ["4NRT660KJQ"], "rxcui": ["1006120"], "spl_set_id": ["cf0cc763-49b5-435d-852b-e7617c8d3286"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE, DROPPER (68788-9871-1)", "package_ndc": "68788-9871-1", "marketing_start_date": "20120228"}], "brand_name": "Sulfacetamide Sodium", "product_id": "68788-9871_fe2e1b1d-4502-43a2-90f5-7b06d074ac1b", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "68788-9871", "generic_name": "sulfacetamide sodium", "labeler_name": "Preferred Pharmaceuticals, 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": "20120228", "listing_expiration_date": "20261231"}