sodium sulfacetamide
Generic: sodium sulfacetamide
Labeler: oceanside pharmaceuticalsDrug Facts
Product Profile
Brand Name
sodium sulfacetamide
Generic Name
sodium sulfacetamide
Labeler
oceanside pharmaceuticals
Dosage Form
LOTION
Routes
Active Ingredients
sulfacetamide sodium 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68682-010
Product ID
68682-010_4dcab06b-56fb-4e42-aae0-6e8840ddd80a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA019931
Listing Expiration
2026-12-31
Marketing Start
2015-12-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68682010
Hyphenated Format
68682-010
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
sodium sulfacetamide (source: ndc)
Generic Name
sodium sulfacetamide (source: ndc)
Application Number
NDA019931 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (68682-010-04) / 118 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4dcab06b-56fb-4e42-aae0-6e8840ddd80a", "openfda": {"unii": ["4NRT660KJQ"], "rxcui": ["1006688"], "spl_set_id": ["6fa7399b-4ced-492d-b6f6-cf155764087a"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68682-010-04) / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "68682-010-04", "marketing_start_date": "20151218"}], "brand_name": "Sodium sulfacetamide", "product_id": "68682-010_4dcab06b-56fb-4e42-aae0-6e8840ddd80a", "dosage_form": "LOTION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "68682-010", "generic_name": "Sodium sulfacetamide", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium sulfacetamide", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}], "application_number": "NDA019931", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20151218", "listing_expiration_date": "20261231"}