methylprednisolone sodium succinate

Generic: methylprednisolone sodium succinate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylprednisolone sodium succinate
Generic Name methylprednisolone sodium succinate
Labeler remedyrepack inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

methylprednisolone sodium succinate 125 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4345
Product ID 70518-4345_36218d0a-50c8-3843-e063-6394a90aa28e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203125
Listing Expiration 2026-12-31
Marketing Start 2025-05-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184345
Hyphenated Format 70518-4345

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 methylprednisolone sodium succinate (source: ndc)
Generic Name methylprednisolone sodium succinate (source: ndc)
Application Number ANDA203125 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4345-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (70518-4345-1)
source: ndc

Packages (1)

70518-4345-0 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4345-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (70518-4345-1)

Ingredients (1)

methylprednisolone sodium succinate (125 mg/1)

Linked Drug Pages (1)

Methylprednisolone Sodium Succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "36218d0a-50c8-3843-e063-6394a90aa28e", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["1743704"], "spl_set_id": ["ae524bdb-9fd0-49f9-802d-465a374c175b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4345-0)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (70518-4345-1)", "package_ndc": "70518-4345-0", "marketing_start_date": "20250527"}], "brand_name": "Methylprednisolone Sodium Succinate", "product_id": "70518-4345_36218d0a-50c8-3843-e063-6394a90aa28e", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-4345", "generic_name": "Methylprednisolone Sodium Succinate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone Sodium Succinate", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "125 mg/1"}], "application_number": "ANDA203125", "marketing_category": "ANDA", "marketing_start_date": "20250527", "listing_expiration_date": "20261231"}