solu-medrol

Generic: solu-medrol

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

Drug Facts

Product Profile

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

methylprednisolone sodium succinate 125 mg/2mL

Manufacturer
HF Acquisition Co. LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1263
Product ID 51662-1263_101f02e1-5d9f-7fc6-e063-6294a90a1455
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA011856
Listing Expiration 2026-12-31
Marketing Start 2018-09-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621263
Hyphenated Format 51662-1263

Supplemental Identifiers

RxCUI
1743704
UNII
LEC9GKY20K

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-medrol (source: ndc)
Generic Name solu-medrol (source: ndc)
Application Number NDA011856 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 125 mg/2mL
source: ndc
Packaging
  • 1 mL in 1 VIAL, SINGLE-USE (51662-1263-1)
  • 25 POUCH in 1 CASE (51662-1263-3) / 1 mL in 1 POUCH (51662-1263-2)
source: ndc

Packages (2)

51662-1263-1 1 mL in 1 VIAL, SINGLE-USE (51662-1263-1) 51662-1263-3 25 POUCH in 1 CASE (51662-1263-3) / 1 mL in 1 POUCH (51662-1263-2)

Ingredients (1)

methylprednisolone sodium succinate (125 mg/2mL)

Linked Drug Pages (1)

SOLU-MEDROL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "101f02e1-5d9f-7fc6-e063-6294a90a1455", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["1743704"], "spl_set_id": ["74e448ed-f4b4-8d09-e053-2991aa0a7500"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-USE (51662-1263-1)", "package_ndc": "51662-1263-1", "marketing_start_date": "20180902"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1263-3)  / 1 mL in 1 POUCH (51662-1263-2)", "package_ndc": "51662-1263-3", "marketing_start_date": "20200429"}], "brand_name": "SOLU-MEDROL", "product_id": "51662-1263_101f02e1-5d9f-7fc6-e063-6294a90a1455", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51662-1263", "generic_name": "SOLU-MEDROL", "labeler_name": "HF Acquisition Co. LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOLU-MEDROL", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "125 mg/2mL"}], "application_number": "NDA011856", "marketing_category": "NDA", "marketing_start_date": "20180902", "listing_expiration_date": "20261231"}