solu-medrol
Generic: methylprednisolone sodium succinate
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
solu-medrol
Generic Name
methylprednisolone sodium succinate
Labeler
propharma distribution
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
methylprednisolone sodium succinate 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84549-039
Product ID
84549-039_463eae7b-ee0e-b775-e063-6394a90ae2c3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA011856
Listing Expiration
2026-12-31
Marketing Start
1959-04-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549039
Hyphenated Format
84549-039
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 1 mL in 1 VIAL (84549-039-28)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "463eae7b-ee0e-b775-e063-6394a90ae2c3", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["207191", "311659"], "spl_set_id": ["42df21df-9284-4505-e063-6294a90a7024"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (84549-039-28)", "package_ndc": "84549-039-28", "marketing_start_date": "20251010"}], "brand_name": "SOLU-MEDROL", "product_id": "84549-039_463eae7b-ee0e-b775-e063-6394a90ae2c3", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "84549-039", "generic_name": "methylprednisolone sodium succinate", "labeler_name": "ProPharma Distribution", "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"}