prednisolone sodium phosphate
Generic: prednisolone sodium phosphate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
prednisolone sodium phosphate
Generic Name
prednisolone sodium phosphate
Labeler
proficient rx lp
Dosage Form
SOLUTION
Routes
Active Ingredients
prednisolone sodium phosphate 15 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
63187-215
Product ID
63187-215_10b381fc-624f-485b-a31f-15d46600232d
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
63187215
Hyphenated Format
63187-215
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
- 240 mL in 1 BOTTLE (63187-215-64)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "10b381fc-624f-485b-a31f-15d46600232d", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["14b7f41b-4df1-42cb-bd1b-c74b28de2670"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (63187-215-64)", "package_ndc": "63187-215-64", "marketing_start_date": "20140901"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "63187-215_10b381fc-624f-485b-a31f-15d46600232d", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "63187-215", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "Proficient Rx LP", "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"}