Package 0121-0773-08

Brand: prednisolone sodium phosphate

Generic: prednisolone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 0121-0773-08
Digits Only 0121077308
Product NDC 0121-0773
Product ID 0121-0773_cdc1335b-41fb-4df2-b201-69150adbb03d
Description

237 mL in 1 BOTTLE (0121-0773-08)

Marketing

Marketing Status
Marketed Since 2017-01-31
Brand prednisolone sodium phosphate
Generic prednisolone sodium phosphate
Sample Package No

Linked Drug Pages (1)

Prednisolone Sodium Phosphate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cdc1335b-41fb-4df2-b201-69150adbb03d", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["794979"], "spl_set_id": ["93cd0ddd-1cf5-4064-9a4c-015819c0065a"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (0121-0773-08)", "package_ndc": "0121-0773-08", "marketing_start_date": "20170131"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "0121-0773_cdc1335b-41fb-4df2-b201-69150adbb03d", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0121-0773", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisolone Sodium Phosphate", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "10 mg/5mL"}], "application_number": "ANDA078465", "marketing_category": "ANDA", "marketing_start_date": "20170131", "listing_expiration_date": "20261231"}