sulfacetamide sodium

Generic: sulfacetamide sodium

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sulfacetamide sodium
Generic Name sulfacetamide sodium
Labeler asclemed usa, inc.
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

sulfacetamide sodium 100 mg/mL

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-090
Product ID 76420-090_b26a1d2a-bf50-4787-e053-2a95a90a951b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040066
Listing Expiration 2026-12-31
Marketing Start 1994-12-28

Pharmacologic Class

Classes
sulfonamide antibacterial [epc] sulfonamides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420090
Hyphenated Format 76420-090

Supplemental Identifiers

RxCUI
1006120
UNII
4NRT660KJQ

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
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
Packaging
  • 15 mL in 1 BOTTLE, DROPPER (76420-090-15)
source: ndc

Packages (1)

Ingredients (1)

sulfacetamide sodium (100 mg/mL)

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"}