prednisolone sodium phosphate
Generic: prednisolone sodium phosphate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
prednisolone sodium phosphate
Generic Name
prednisolone sodium phosphate
Labeler
a-s medication solutions
Dosage Form
SOLUTION
Routes
Active Ingredients
prednisolone sodium phosphate 15 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-1582
Product ID
50090-1582_9cdcdc91-0b2c-43eb-9891-a581be9bdb30
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076913
Listing Expiration
2026-12-31
Marketing Start
2005-04-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500901582
Hyphenated Format
50090-1582
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 15 mg/5mL
Packaging
- 237 mL in 1 BOTTLE (50090-1582-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9cdcdc91-0b2c-43eb-9891-a581be9bdb30", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["4c507319-8add-4952-8bea-ff77ab17088f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (50090-1582-0)", "package_ndc": "50090-1582-0", "marketing_start_date": "20141229"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "50090-1582_9cdcdc91-0b2c-43eb-9891-a581be9bdb30", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-1582", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "A-S Medication Solutions", "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": "20050425", "listing_expiration_date": "20261231"}