solu-medrol

Generic: methylprednisolone sodium succinate

Labeler: pharmacia & upjohn company llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name solu-medrol
Generic Name methylprednisolone sodium succinate
Labeler pharmacia & upjohn company llc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

methylprednisolone sodium succinate 40 mg/mL

Manufacturer
Pharmacia & Upjohn Company LLC

Identifiers & Regulatory

Product NDC 0009-0039
Product ID 0009-0039_c157d266-8633-4c2e-ae1f-0207e4f19b35
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA011856
Listing Expiration 2026-12-31
Marketing Start 1959-04-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00090039
Hyphenated Format 0009-0039

Supplemental Identifiers

RxCUI
207191 207193 311659 314099 1357886 1357888 1743704 1743707 1743720 1743722 1743726 1743729
UNII
LEC9GKY20K

Packaging Origin

Original Packager
true

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 methylprednisolone sodium succinate (source: ndc)
Application Number NDA011856 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (0009-0039-28) / 1 mL in 1 VIAL (0009-0039-30)
  • 25 VIAL in 1 CARTON (0009-0039-32) / 1 mL in 1 VIAL (0009-0039-33)
source: ndc

Packages (2)

0009-0039-28 25 VIAL in 1 CARTON (0009-0039-28) / 1 mL in 1 VIAL (0009-0039-30) 0009-0039-32 25 VIAL in 1 CARTON (0009-0039-32) / 1 mL in 1 VIAL (0009-0039-33)

Ingredients (1)

methylprednisolone sodium succinate (40 mg/mL)

Linked Drug Pages (2)

SOLU-MEDROL ndc-match (0.9) SOLU-MEDROL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "c157d266-8633-4c2e-ae1f-0207e4f19b35", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["207191", "207193", "311659", "314099", "1357886", "1357888", "1743704", "1743707", "1743720", "1743722", "1743726", "1743729"], "spl_set_id": ["cd99be87-c8d9-48d6-a8e5-e081052e3f19"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0009-0039-28)  / 1 mL in 1 VIAL (0009-0039-30)", "package_ndc": "0009-0039-28", "marketing_start_date": "19590402"}, {"sample": false, "description": "25 VIAL in 1 CARTON (0009-0039-32)  / 1 mL in 1 VIAL (0009-0039-33)", "package_ndc": "0009-0039-32", "marketing_start_date": "19590402"}], "brand_name": "SOLU-MEDROL", "product_id": "0009-0039_c157d266-8633-4c2e-ae1f-0207e4f19b35", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0009-0039", "generic_name": "methylprednisolone sodium succinate", "labeler_name": "Pharmacia & Upjohn Company LLC", "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": "19590402", "listing_expiration_date": "20261231"}