prednisolone sodium phosphate

Generic: prednisolone sodium phosphate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisolone sodium phosphate
Generic Name prednisolone sodium phosphate
Labeler remedyrepack inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

prednisolone sodium phosphate 15 mg/5mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4524
Product ID 70518-4524_4a78234e-7fc3-5901-e063-6294a90a71c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076913
Listing Expiration 2027-12-31
Marketing Start 2025-11-28

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184524
Hyphenated Format 70518-4524

Supplemental Identifiers

RxCUI
283077
UNII
IV021NXA9J

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 prednisolone sodium phosphate (source: ndc)
Generic Name prednisolone sodium phosphate (source: ndc)
Application Number ANDA076913 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/5mL
source: ndc
Packaging
  • 2 CUP in 1 BOX (70518-4524-0) / 25 mL in 1 CUP (70518-4524-1)
  • 5 CUP in 1 BOX (70518-4524-2) / 10 mL in 1 CUP (70518-4524-3)
  • 10 CUP in 1 BOX (70518-4524-4) / 5 mL in 1 CUP (70518-4524-5)
source: ndc

Packages (3)

70518-4524-0 2 CUP in 1 BOX (70518-4524-0) / 25 mL in 1 CUP (70518-4524-1) 70518-4524-2 5 CUP in 1 BOX (70518-4524-2) / 10 mL in 1 CUP (70518-4524-3) 70518-4524-4 10 CUP in 1 BOX (70518-4524-4) / 5 mL in 1 CUP (70518-4524-5)

Ingredients (1)

prednisolone sodium phosphate (15 mg/5mL)

Linked Drug Pages (1)

Prednisolone Sodium Phosphate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a78234e-7fc3-5901-e063-6294a90a71c3", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["f87ce1ba-335e-463d-87d5-9af0206f8f61"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "2 CUP in 1 BOX (70518-4524-0)  / 25 mL in 1 CUP (70518-4524-1)", "package_ndc": "70518-4524-0", "marketing_start_date": "20251128"}, {"sample": false, "description": "5 CUP in 1 BOX (70518-4524-2)  / 10 mL in 1 CUP (70518-4524-3)", "package_ndc": "70518-4524-2", "marketing_start_date": "20251210"}, {"sample": false, "description": "10 CUP in 1 BOX (70518-4524-4)  / 5 mL in 1 CUP (70518-4524-5)", "package_ndc": "70518-4524-4", "marketing_start_date": "20260209"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "70518-4524_4a78234e-7fc3-5901-e063-6294a90a71c3", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-4524", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisolone Sodium Phosphate", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "15 mg/5mL"}], "application_number": "ANDA076913", "marketing_category": "ANDA", "marketing_start_date": "20251128", "listing_expiration_date": "20271231"}