prednisolone sodium phosphate
Generic: prednisolone sodium phosphate
Labeler: redpharm drugDrug Facts
Product Profile
Brand Name
prednisolone sodium phosphate
Generic Name
prednisolone sodium phosphate
Labeler
redpharm drug
Dosage Form
SOLUTION
Routes
Active Ingredients
prednisolone sodium phosphate 15 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
67296-2134
Product ID
67296-2134_46aca408-309a-ee64-e063-6294a90a5f4d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203559
Listing Expiration
2026-12-31
Marketing Start
2023-10-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
672962134
Hyphenated Format
67296-2134
Supplemental Identifiers
RxCUI
UPC
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
ANDA203559 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 mg/5mL
Packaging
- 60 mL in 1 BOTTLE, PLASTIC (67296-2134-6)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46aca408-309a-ee64-e063-6294a90a5f4d", "openfda": {"upc": ["0342799813011", "0342799816012", "0342799815015", "0342799812014"], "unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["3253b63b-0533-6cdc-e063-6294a90aa311"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE, PLASTIC (67296-2134-6)", "package_ndc": "67296-2134-6", "marketing_start_date": "20231009"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "67296-2134_46aca408-309a-ee64-e063-6294a90a5f4d", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "67296-2134", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisolone Sodium Phosphate", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "15 mg/5mL"}], "application_number": "ANDA203559", "marketing_category": "ANDA", "marketing_start_date": "20231009", "listing_expiration_date": "20261231"}