Package 0121-0759-08

Brand: prednisolone sodium phosphate

Generic: prednisolone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 0121-0759-08
Digits Only 0121075908
Product NDC 0121-0759
Product ID 0121-0759_07592713-8b0b-47aa-8a7f-848823ff221c
Description

237 mL in 1 BOTTLE (0121-0759-08)

Marketing

Marketing Status
Marketed Since 2005-04-25
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": "07592713-8b0b-47aa-8a7f-848823ff221c", "openfda": {"upc": ["0301210759086"], "unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["a0d74ae0-7b2d-4d36-9211-c76f5063b5a9"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (0121-0759-08)", "package_ndc": "0121-0759-08", "marketing_start_date": "20050425"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "0121-0759_07592713-8b0b-47aa-8a7f-848823ff221c", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0121-0759", "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": "15 mg/5mL"}], "application_number": "ANDA076913", "marketing_category": "ANDA", "marketing_start_date": "20050425", "listing_expiration_date": "20261231"}