Package 84549-011-04

Brand: solu-cortef

Generic: hydrocortisone sodium succinate
NDC Package

Package Facts

Identity

Package NDC 84549-011-04
Digits Only 8454901104
Product NDC 84549-011
Product ID 84549-011_3a38d1c4-e75c-f6e9-e063-6394a90a888b
Description

2 mL in 1 VIAL, SINGLE-DOSE (84549-011-04)

Marketing

Marketing Status
Marketed Since 2025-08-27
Brand solu-cortef
Generic hydrocortisone sodium succinate
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": "3a38d1c4-e75c-f6e9-e063-6394a90a888b", "openfda": {"unii": ["50LQB69S1Z"], "rxcui": ["105398", "238755"], "spl_set_id": ["386942d3-c75f-25f1-e063-6394a90a5af2"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, SINGLE-DOSE (84549-011-04)", "package_ndc": "84549-011-04", "marketing_start_date": "20250827"}], "brand_name": "Solu-Cortef", "product_id": "84549-011_3a38d1c4-e75c-f6e9-e063-6394a90a888b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "84549-011", "generic_name": "hydrocortisone sodium succinate", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Solu-Cortef", "active_ingredients": [{"name": "HYDROCORTISONE SODIUM SUCCINATE", "strength": "100 mg/2mL"}], "application_number": "NDA009866", "marketing_category": "NDA", "marketing_start_date": "19550427", "listing_expiration_date": "20261231"}