solu-cortef

Generic: solu-cortef

Labeler: hf acquisition co. llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name solu-cortef
Generic Name solu-cortef
Labeler hf acquisition co. llc, dba healthfirst
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

hydrocortisone sodium succinate 100 mg/2mL

Manufacturer
HF Acquisition Co. LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1261
Product ID 51662-1261_1203ca7f-080b-4c49-e063-6294a90a90e0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA009866
Listing Expiration 2026-12-31
Marketing Start 2018-09-03

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621261
Hyphenated Format 51662-1261

Supplemental Identifiers

RxCUI
238755
UNII
50LQB69S1Z

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name solu-cortef (source: ndc)
Generic Name solu-cortef (source: ndc)
Application Number NDA009866 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/2mL
source: ndc
Packaging
  • 2 mL in 1 VIAL, SINGLE-DOSE (51662-1261-1)
  • 25 POUCH in 1 CASE (51662-1261-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1261-2) / 2 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

51662-1261-1 2 mL in 1 VIAL, SINGLE-DOSE (51662-1261-1) 51662-1261-3 25 POUCH in 1 CASE (51662-1261-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1261-2) / 2 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

hydrocortisone sodium succinate (100 mg/2mL)

Linked Drug Pages (1)

SOLU-CORTEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "1203ca7f-080b-4c49-e063-6294a90a90e0", "openfda": {"unii": ["50LQB69S1Z"], "rxcui": ["238755"], "spl_set_id": ["74f84173-a43f-7788-e053-2991aa0a8fb2"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, SINGLE-DOSE (51662-1261-1)", "package_ndc": "51662-1261-1", "marketing_start_date": "20180903"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1261-3)  / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1261-2)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1261-3", "marketing_start_date": "20221110"}], "brand_name": "SOLU-CORTEF", "product_id": "51662-1261_1203ca7f-080b-4c49-e063-6294a90a90e0", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51662-1261", "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": "100 mg/2mL"}], "application_number": "NDA009866", "marketing_category": "NDA", "marketing_start_date": "20180903", "listing_expiration_date": "20261231"}