prednisolone sodium phosphate
Generic: prednisolone sodium phosphate
Labeler: preferred pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
prednisolone sodium phosphate
Generic Name
prednisolone sodium phosphate
Labeler
preferred pharmaceuticals, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
prednisolone sodium phosphate 15 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7708
Product ID
68788-7708_1093c0d9-480a-496c-b84d-3e9a34d74845
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076913
Listing Expiration
2026-12-31
Marketing Start
2020-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887708
Hyphenated Format
68788-7708
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 (68788-7708-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1093c0d9-480a-496c-b84d-3e9a34d74845", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["93b372f7-b811-4c15-85c4-c6dbac342cb4"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (68788-7708-2)", "package_ndc": "68788-7708-2", "marketing_start_date": "20200601"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "68788-7708_1093c0d9-480a-496c-b84d-3e9a34d74845", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-7708", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "Preferred Pharmaceuticals, 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": "20200601", "listing_expiration_date": "20261231"}