Package 68788-7708-2

Brand: prednisolone sodium phosphate

Generic: prednisolone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 68788-7708-2
Digits Only 6878877082
Product NDC 68788-7708
Description

237 mL in 1 BOTTLE (68788-7708-2)

Marketing

Marketing Status
Marketed Since 2020-06-01
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": "1093c0d9-480a-496c-b84d-3e9a34d74845", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["93b372f7-b811-4c15-85c4-c6dbac342cb4"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (68788-7708-2)", "package_ndc": "68788-7708-2", "marketing_start_date": "20200601"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "68788-7708_1093c0d9-480a-496c-b84d-3e9a34d74845", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-7708", "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": "ANDA076913", "marketing_category": "ANDA", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}