sulfacetamide sodium and prednisolone sodium phosphate

Generic: sulfacetamide sodium and prednisolone sodium phosphate

Labeler: bausch & lomb incoporated
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug 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
OPHTHALMIC
Active Ingredients

prednisolone sodium phosphate 2.3 mg/mL, sulfacetamide sodium 100 mg/mL

Manufacturer
Bausch & Lomb Incoporated

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
corticosteroid hormone receptor agonists [moa] corticosteroid [epc] sulfonamide antibacterial [epc] sulfonamides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208317
Hyphenated Format 24208-317

Supplemental Identifiers

RxCUI
1012021
UNII
IV021NXA9J 4NRT660KJQ

Packaging Origin

Original Packager
true

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
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 2.3 mg/mL
  • 100 mg/mL
source: ndc
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
source: ndc

Packages (2)

Ingredients (2)

prednisolone sodium phosphate (2.3 mg/mL) sulfacetamide sodium (100 mg/mL)

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"}