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Data / Drug companies / Methylprednisolone acetate

Methylprednisolone acetate: 10 companies and 36 products in the FDA NDC directory

Methylprednisolone acetate is listed in the FDA National Drug Code Directory by 10 companies, with 36 products in commercial distribution. 22 of the products (61.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, suspension, and the newest product started marketing on November 2, 2026.

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Companies listing it
10
Products
36
Generic (ANDA) products
22 (61.1%)
Application numbers
7
Routes
Intralesional, Intramuscular, Soft tissue, Intra-articular, Intrasynovial
Brand names
Depo-Medrol, Depo-Medrol, Medroloan II Suik, Medroloan Suik
openFDA record search
api.fda.gov

Companies that list methylprednisolone acetate

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions6injection, suspensionNew drug applications (NDA)May 20, 2019
Pharmacia & Upjohn Company LLC6injection, suspensionNew drug applications (NDA)May 28, 1959
Amneal Pharmaceuticals LLC5injection, suspensionGeneric drugs (ANDA)November 10, 2023
Gland Pharma Limited5injection, suspensionGeneric drugs (ANDA)November 2, 2026
Asclemed USA, Inc.3injection, suspensionOther unapproved drugsJune 29, 2016
Sportpharm LLC3injection, suspensionGeneric drugs (ANDA)November 15, 2021
Amneal Pharmaceuticals NY LLC2injection, suspensionGeneric drugs (ANDA)April 10, 2022
Caplin Steriles Limited2injection, suspensionGeneric drugs (ANDA)February 6, 2026
Eugia US LLC2injection, suspensionGeneric drugs (ANDA)April 13, 2023
Sagent Pharmaceuticals2injection, suspensionGeneric drugs (ANDA)November 15, 2021

Dosage forms

Dosage formProductsShare
Injection, suspension36100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)2261.1%
New drug applications (NDA)1233.3%
Other unapproved drugs25.6%

Pharmacologic classes

ClassProducts
Corticosteroid36

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.