Package 68788-4046-2

Brand: prednisolone sodium phosphate

Generic: prednisolone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 68788-4046-2
Digits Only 6878840462
Product NDC 68788-4046
Description

237 mL in 1 BOTTLE, PLASTIC (68788-4046-2)

Marketing

Marketing Status
Marketed Since 2025-10-28
Brand prednisolone sodium phosphate
Generic prednisolone sodium phosphate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7262fc84-3db2-4475-8ae4-6bec4477cb81", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["7262fc84-3db2-4475-8ae4-6bec4477cb81"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (68788-4046-2)", "package_ndc": "68788-4046-2", "marketing_start_date": "20251028"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "68788-4046_7262fc84-3db2-4475-8ae4-6bec4477cb81", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-4046", "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": "ANDA203559", "marketing_category": "ANDA", "marketing_start_date": "20251028", "listing_expiration_date": "20261231"}