methylprednisolone sodium succinate (0143-9754)

Drug Facts

Product Profile

Brand Name methylprednisolone sodium succinate

Generic Name methylprednisolone sodium succinate

Labeler hikma pharmaceuticals usa inc.

Dosage Form INJECTION, POWDER, FOR SOLUTION

Routes

INTRAMUSCULAR INTRAVENOUS

Active Ingredients

methylprednisolone sodium succinate 125 mg/1

Manufacturer

Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9754

Product ID 0143-9754_7700d2a0-e17c-49e4-96ea-956742ed0e70

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA203125

Listing Expiration 2026-12-31

Marketing Start 2022-09-26

Pharmacologic Class

Classes

corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439754

Hyphenated Format 0143-9754

Supplemental Identifiers

RxCUI

311659 1743704

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 ANDA203125 (source: ndc)

Routes

INTRAMUSCULAR INTRAVENOUS

source: ndc

Resolved Composition

Strengths

125 mg/1

source: ndc

Packaging

25 VIAL, SINGLE-DOSE in 1 CARTON (0143-9754-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0143-9754-01)

source: ndc

Packages (1)

0143-9754-25 25 VIAL, SINGLE-DOSE in 1 CARTON (0143-9754-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0143-9754-01)

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": "7700d2a0-e17c-49e4-96ea-956742ed0e70", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["311659", "1743704"], "spl_set_id": ["05d95a56-b03a-4d5b-9877-2853ac470fa1"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (0143-9754-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0143-9754-01)", "package_ndc": "0143-9754-25", "marketing_start_date": "20220926"}], "brand_name": "Methylprednisolone Sodium Succinate", "product_id": "0143-9754_7700d2a0-e17c-49e4-96ea-956742ed0e70", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0143-9754", "generic_name": "Methylprednisolone Sodium Succinate", "labeler_name": "Hikma Pharmaceuticals USA 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": "20220926", "listing_expiration_date": "20261231"}