methylprednisolone sodium succinate (55150-264)

Drug Facts

Product Profile

Brand Name methylprednisolone sodium succinate

Generic Name methylprednisolone sodium succinate

Labeler eugia us llc

Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Routes

INTRAMUSCULAR INTRAVENOUS

Active Ingredients

methylprednisolone sodium succinate 500 mg/1

Manufacturer

Eugia US LLC

Identifiers & Regulatory

Product NDC 55150-264

Product ID 55150-264_1d8c98fc-8bb8-4caa-a745-5d42ddd2c8ec

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA207667

Listing Expiration 2026-12-31

Marketing Start 2015-12-15

Pharmacologic Class

Classes

corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55150264

Hyphenated Format 55150-264

Supplemental Identifiers

RxCUI

311659 314099 1357886 1743704

UPC

0355150265503 0355150264209

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 methylprednisolone sodium succinate (source: ndc)

Generic Name methylprednisolone sodium succinate (source: ndc)

Application Number ANDA207667 (source: ndc)

Routes

INTRAMUSCULAR INTRAVENOUS

source: ndc

Resolved Composition

Strengths

500 mg/1

source: ndc

Packaging

1 VIAL, MULTI-DOSE in 1 CARTON (55150-264-20) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, MULTI-DOSE

source: ndc

Packages (1)

55150-264-20 1 VIAL, MULTI-DOSE in 1 CARTON (55150-264-20) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, MULTI-DOSE

Ingredients (1)

methylprednisolone sodium succinate (500 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": "1d8c98fc-8bb8-4caa-a745-5d42ddd2c8ec", "openfda": {"upc": ["0355150265503", "0355150264209"], "unii": ["LEC9GKY20K"], "rxcui": ["311659", "314099", "1357886", "1743704"], "spl_set_id": ["2035f00e-2299-473a-b004-cb93f541cfa9"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (55150-264-20)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-264-20", "marketing_start_date": "20151215"}], "brand_name": "Methylprednisolone Sodium Succinate", "product_id": "55150-264_1d8c98fc-8bb8-4caa-a745-5d42ddd2c8ec", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "55150-264", "generic_name": "Methylprednisolone Sodium Succinate", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone Sodium Succinate", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "500 mg/1"}], "application_number": "ANDA207667", "marketing_category": "ANDA", "marketing_start_date": "20151215", "listing_expiration_date": "20261231"}