Package 17856-8815-1

Brand: prednisolone sodium phosphate

Generic: prednisolone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 17856-8815-1
Digits Only 1785688151
Product NDC 17856-8815
Description

50 CUP, UNIT-DOSE in 1 CASE (17856-8815-1) / 5 mL in 1 CUP, UNIT-DOSE

Marketing

Marketing Status
Marketed Since 2025-10-01
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": "401f96d7-592c-5df2-e063-6294a90a104d", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["401f7ba6-a4a2-9ae6-e063-6394a90a4210"], "manufacturer_name": ["Atlantic Biologicals Corp"]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (17856-8815-1)  / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-8815-1", "marketing_start_date": "20251001"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "17856-8815_401f96d7-592c-5df2-e063-6294a90a104d", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "17856-8815", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "Atlantic Biologicals Corp", "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"}