solu-medrol
Generic: methylprednisolone sodium succinate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
solu-medrol
Generic Name
methylprednisolone sodium succinate
Labeler
remedyrepack inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
methylprednisolone sodium succinate 125 mg/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-2023
Product ID
70518-2023_499b1561-882b-8553-e063-6294a90ad423
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA011856
Listing Expiration
2027-12-31
Marketing Start
2019-04-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705182023
Hyphenated Format
70518-2023
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
- 125 mg/2mL
Packaging
- 25 VIAL in 1 CARTON (70518-2023-1) / 2 mL in 1 VIAL (70518-2023-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "499b1561-882b-8553-e063-6294a90ad423", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["1743704", "1743707"], "spl_set_id": ["1d5ef347-2e9a-432f-9a88-a7c4ba300267"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70518-2023-1) / 2 mL in 1 VIAL (70518-2023-0)", "package_ndc": "70518-2023-1", "marketing_start_date": "20190415"}], "brand_name": "SOLU-MEDROL", "product_id": "70518-2023_499b1561-882b-8553-e063-6294a90ad423", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-2023", "generic_name": "methylprednisolone sodium succinate", "labeler_name": "REMEDYREPACK INC.", "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": "20190415", "listing_expiration_date": "20271231"}