prednisolone sodium phosphate
Generic: prednisolone sodium phosphate
Labeler: edenbridge pharmaceuticals llc.Drug Facts
Product Profile
Brand Name
prednisolone sodium phosphate
Generic Name
prednisolone sodium phosphate
Labeler
edenbridge pharmaceuticals llc.
Dosage Form
SOLUTION
Routes
Active Ingredients
prednisolone sodium phosphate 15 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
42799-815
Product ID
42799-815_462f70d9-438c-e6b2-e063-6394a90a1bbb
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
42799815
Hyphenated Format
42799-815
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
- 237 mL in 1 BOTTLE, PLASTIC (42799-815-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "462f70d9-438c-e6b2-e063-6394a90a1bbb", "openfda": {"upc": ["0342799813011", "0342799816012", "0342799815015", "0342799812014"], "unii": ["IV021NXA9J"], "rxcui": ["249066", "283077", "702306", "794979"], "spl_set_id": ["1793e218-7b49-497d-879f-1020de6e6d68"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (42799-815-01)", "package_ndc": "42799-815-01", "marketing_start_date": "20231009"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "42799-815_462f70d9-438c-e6b2-e063-6394a90a1bbb", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "42799-815", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "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"}