sulfacetamide sodium and prednisolone sodium phosphate
Generic: sulfacetamide sodium and prednisolone sodium phosphate
Labeler: bausch & lomb incoporatedDrug Facts
Product Profile
Brand Name
sulfacetamide sodium and prednisolone sodium phosphate
Generic Name
sulfacetamide sodium and prednisolone sodium phosphate
Labeler
bausch & lomb incoporated
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
prednisolone sodium phosphate 2.3 mg/mL, sulfacetamide sodium 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24208-317
Product ID
24208-317_06ea3d35-67bf-d0b8-e063-6294a90a5b0c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074449
Listing Expiration
2026-12-31
Marketing Start
1995-12-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24208317
Hyphenated Format
24208-317
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 and prednisolone sodium phosphate (source: ndc)
Generic Name
sulfacetamide sodium and prednisolone sodium phosphate (source: ndc)
Application Number
ANDA074449 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.3 mg/mL
- 100 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (24208-317-05) / 5 mL in 1 BOTTLE, DROPPER
- 1 BOTTLE, DROPPER in 1 CARTON (24208-317-10) / 10 mL in 1 BOTTLE, DROPPER
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "06ea3d35-67bf-d0b8-e063-6294a90a5b0c", "openfda": {"unii": ["IV021NXA9J", "4NRT660KJQ"], "rxcui": ["1012021"], "spl_set_id": ["9ec403eb-b5df-4e41-9e17-9d9d8ecac3f3"], "manufacturer_name": ["Bausch & Lomb Incoporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-317-05) / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-317-05", "marketing_start_date": "19951229"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-317-10) / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-317-10", "marketing_start_date": "19951229"}], "brand_name": "Sulfacetamide Sodium and Prednisolone Sodium Phosphate", "product_id": "24208-317_06ea3d35-67bf-d0b8-e063-6294a90a5b0c", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "24208-317", "generic_name": "Sulfacetamide Sodium and Prednisolone Sodium Phosphate", "labeler_name": "Bausch & Lomb Incoporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sulfacetamide Sodium and Prednisolone Sodium Phosphate", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "2.3 mg/mL"}, {"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}], "application_number": "ANDA074449", "marketing_category": "ANDA", "marketing_start_date": "19951229", "listing_expiration_date": "20261231"}