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 40 mg/mL

Manufacturer
HF Acquisition Co. LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1264
Product ID 51662-1264_1203ca7f-080c-4c49-e063-6294a90a90e0
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 516621264
Hyphenated Format 51662-1264

Supplemental Identifiers

RxCUI
311659
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
  • 40 mg/mL
source: ndc
Packaging
  • 1 mL in 1 VIAL, SINGLE-DOSE (51662-1264-1)
  • 25 POUCH in 1 CASE (51662-1264-3) / 1 mL in 1 POUCH (51662-1264-2)
source: ndc

Packages (2)

51662-1264-1 1 mL in 1 VIAL, SINGLE-DOSE (51662-1264-1) 51662-1264-3 25 POUCH in 1 CASE (51662-1264-3) / 1 mL in 1 POUCH (51662-1264-2)

Ingredients (1)

methylprednisolone sodium succinate (40 mg/mL)

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": "1203ca7f-080c-4c49-e063-6294a90a90e0", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["311659"], "spl_set_id": ["74e5060c-8426-1b77-e053-2a91aa0a1f13"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (51662-1264-1)", "package_ndc": "51662-1264-1", "marketing_start_date": "20180902"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1264-3)  / 1 mL in 1 POUCH (51662-1264-2)", "package_ndc": "51662-1264-3", "marketing_start_date": "20200428"}], "brand_name": "SOLU-MEDROL", "product_id": "51662-1264_1203ca7f-080c-4c49-e063-6294a90a90e0", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51662-1264", "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": "40 mg/mL"}], "application_number": "NDA011856", "marketing_category": "NDA", "marketing_start_date": "20180902", "listing_expiration_date": "20261231"}