prednisolone sodium phosphate
Generic: prednisolone sodium phosphate
Labeler: chartwell governmental & specialty rx, llc.Drug Facts
Product Profile
Brand Name
prednisolone sodium phosphate
Generic Name
prednisolone sodium phosphate
Labeler
chartwell governmental & specialty rx, llc.
Dosage Form
SOLUTION
Routes
Active Ingredients
prednisolone sodium phosphate 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68999-330
Product ID
68999-330_453ad2a6-3423-b21b-e063-6294a90abb44
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075988
Listing Expiration
2026-12-31
Marketing Start
2004-05-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68999330
Hyphenated Format
68999-330
Supplemental Identifiers
RxCUI
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
ANDA075988 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- 2 TRAY in 1 BOX (68999-330-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-330-05)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "453ad2a6-3423-b21b-e063-6294a90abb44", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["312614"], "spl_set_id": ["5ec401b5-132a-4cd2-8c24-6a5c8b63c2f9"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-330-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-330-05)", "package_ndc": "68999-330-24", "marketing_start_date": "20251126"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "68999-330_453ad2a6-3423-b21b-e063-6294a90abb44", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68999-330", "generic_name": "prednisolone sodium phosphate", "labeler_name": "Chartwell Governmental & Specialty RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisolone Sodium Phosphate", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "5 mg/5mL"}], "application_number": "ANDA075988", "marketing_category": "ANDA", "marketing_start_date": "20040525", "listing_expiration_date": "20261231"}