Package 51662-1262-1

Brand: solu-cortef

Generic: solu-cortef
NDC Package

Package Facts

Identity

Package NDC 51662-1262-1
Digits Only 5166212621
Product NDC 51662-1262
Product ID 51662-1262_11ffdbc5-43f8-e2f2-e063-6294a90a43e0
Description

2 mL in 1 VIAL, SINGLE-DOSE (51662-1262-1)

Marketing

Marketing Status
Marketed Since 2018-09-03
Brand solu-cortef
Generic solu-cortef
Sample Package No

Linked Drug Pages (1)

SOLU-CORTEF ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "11ffdbc5-43f8-e2f2-e063-6294a90a43e0", "openfda": {"unii": ["50LQB69S1Z"], "rxcui": ["1738590"], "spl_set_id": ["74f8ccd6-b263-7cc4-e053-2991aa0a896d"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, SINGLE-DOSE (51662-1262-1)", "package_ndc": "51662-1262-1", "marketing_start_date": "20180903"}], "brand_name": "SOLU-CORTEF", "product_id": "51662-1262_11ffdbc5-43f8-e2f2-e063-6294a90a43e0", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51662-1262", "generic_name": "SOLU-CORTEF", "labeler_name": "HF Acquisition Co. LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOLU-CORTEF", "active_ingredients": [{"name": "HYDROCORTISONE SODIUM SUCCINATE", "strength": "250 mg/2mL"}], "application_number": "NDA009866", "marketing_category": "NDA", "marketing_start_date": "20180903", "listing_expiration_date": "20261231"}