Package 44523-182-08

Brand: prednisolone sodium phosphate oral solution

Generic: prednisolone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 44523-182-08
Digits Only 4452318208
Product NDC 44523-182
Description

237 mL in 1 BOTTLE (44523-182-08)

Marketing

Marketing Status
Marketed Since 2019-10-28
Brand prednisolone sodium phosphate oral solution
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": "450e8d3f-b6f6-5251-e063-6394a90aa439", "openfda": {"upc": ["0344523182080"], "unii": ["IV021NXA9J"], "rxcui": ["249066"], "spl_set_id": ["95208441-1700-5d3f-e053-2a95a90a7da2"], "manufacturer_name": ["BioComp Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (44523-182-08)", "package_ndc": "44523-182-08", "marketing_start_date": "20191028"}], "brand_name": "Prednisolone Sodium Phosphate Oral Solution", "product_id": "44523-182_450e8d3f-b6f6-5251-e063-6394a90aa439", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "44523-182", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "BioComp Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisolone Sodium Phosphate Oral Solution", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "25 mg/5mL"}], "application_number": "ANDA091396", "marketing_category": "ANDA", "marketing_start_date": "20191028", "listing_expiration_date": "20261231"}