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Data / Drug companies / Neostigmine methylsulfate

Neostigmine methylsulfate: 24 companies and 49 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Neostigmine methylsulfate is listed in the FDA National Drug Code Directory by 24 companies, with 49 products in commercial distribution. 41 of the products (83.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection; injection, solution, and the newest product started marketing on November 6, 2023.

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Companies listing it
24
Products
49
Generic (ANDA) products
41 (83.7%)
Application numbers
14
Routes
Intravenous
Brand names
Bloxiverz
openFDA record search
api.fda.gov

Companies that list neostigmine methylsulfate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Hikma Pharmaceuticals USA Inc.5injectionGeneric drugs (ANDA)December 28, 2015
Fresenius Kabi USA, LLC4injection, solutionNew drug applications (NDA)January 8, 2015
Medical Purchasing Solutions, LLC4injectionGeneric drugs (ANDA)January 10, 2022
Amneal Pharmaceuticals LLC2injectionGeneric drugs (ANDA)June 20, 2018
Amphastar Pharmaceuticals, Inc.2injectionGeneric drugs (ANDA)September 25, 2017
Be Pharmaceuticals Inc.2injectionGeneric drugs (ANDA)May 13, 2019
Camber Pharmaceuticals, Inc.2injectionGeneric drugs (ANDA)January 4, 2021
Caplin Steriles Limited2injectionGeneric drugs (ANDA)April 30, 2021
Eugia US LLC2injectionGeneric drugs (ANDA)November 2, 2023
Fresenius Kabi USA, LLC2injection, solutionNew drug applications (NDA)September 18, 2018
Gland Pharma Limited2injectionGeneric drugs (ANDA)October 21, 2019
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.2injectionGeneric drugs (ANDA)November 25, 2022
Indoco Remedies Limited2injectionGeneric drugs (ANDA)November 26, 2021
Meitheal Pharmaceuticals Inc.2injectionGeneric drugs (ANDA)April 5, 2021
Par Health USA, LLC2injectionGeneric drugs (ANDA)April 26, 2017
Somerset Therapeutics, LLC2injectionGeneric drugs (ANDA)January 10, 2022
Xellia Pharmaceuticals USA LLC2injectionGeneric drugs (ANDA)January 10, 2021
Xiromed, LLC2injectionGeneric drugs (ANDA)September 9, 2020
Civica, Inc.1injectionGeneric drugs (ANDA)April 16, 2020
Dr. Reddy's Laboratories Inc.1injection, solutionGeneric drugs (ANDA)July 25, 2022
Exela Pharma Sciences, LLC1injectionNew drug applications (NDA)November 6, 2023
Fresenius Kabi USA, LLC1injection, solutionNew drug applications (NDA)January 8, 2015
HF Acquisition Co LLC, DBA HealthFirst1injectionGeneric drugs (ANDA)June 14, 2021
ProPharma Distribution1injectionGeneric drugs (ANDA)September 9, 2020

Dosage forms

Dosage formProductsShare
Injection4183.7%
Injection, solution816.3%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)4183.7%
New drug applications (NDA)816.3%

Pharmacologic classes

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.