Skip to the page

Data / Drug companies / Bupivacaine hydrochloride

Bupivacaine hydrochloride: 23 companies and 103 products in the FDA NDC directory

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

Bupivacaine hydrochloride is listed in the FDA National Drug Code Directory by 23 companies, with 103 products in commercial distribution. 85 of the products (82.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, solution; injection, and the newest product started marketing on June 24, 2026.

The request: Get every company that lists bupivacaine hydrochloride in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
23
Products
103
Generic (ANDA) products
85 (82.5%)
Application numbers
21
Routes
Perineural, Epidural, Intracaudal, Infiltration, Retrobulbar
Brand names
Marcaine, Sensorcaine MPF, Bupivacaine HCl, Sensorcaine MPF, Sensorcaine, Sensorcaine, Marvona Suik, Marvona-25 Suik
openFDA record search
api.fda.gov

Companies that list bupivacaine hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Hospira, Inc.12injection, solutionGeneric drugs (ANDA)August 28, 2025
Fresenius Kabi USA, LLC11injection, solutionNew drug applications (NDA)November 19, 2010
Eugia US LLC8injection, solutionGeneric drugs (ANDA)May 13, 2016
Hikma Pharmaceuticals USA Inc.8injection, solutionGeneric drugs (ANDA)February 11, 2021
NorthStar RxLLC8injection, solutionGeneric drugs (ANDA)December 16, 2024
Onesource Specialty Pharma Limited8injection, solutionGeneric drugs (ANDA)January 29, 2026
Xellia Pharmaceuticals USA LLC8injection, solutionGeneric drugs (ANDA)August 1, 2023
Henry Schein, Inc.7injection, solutionNew drug applications (NDA)June 24, 2026
Anthea Pharma Private Limited5injection, solutionGeneric drugs (ANDA)April 22, 2026
Asclemed USA, Inc.5injection, solutionGeneric drugs (ANDA)February 11, 2021
Camber Pharmaceuticals, Inc.3injection, solutionGeneric drugs (ANDA)March 27, 2024
Medical Purchasing Solutions, LLC3injection, solutionGeneric drugs (ANDA)May 13, 2016
Sportpharm LLC3injection, solutionGeneric drugs (ANDA)May 13, 2016
Fosun Pharma USA Inc.2injection, solutionGeneric drugs (ANDA)February 6, 2026
Meitheal Pharmaceuticals Inc.2injection, solutionGeneric drugs (ANDA)June 23, 2023
ProPharma Distribution2injection, solutionGeneric drugs (ANDA)November 22, 2005
Somerset Therapeutics, LLC2injection, solutionGeneric drugs (ANDA)November 27, 2023
A-S Medication Solutions1injection, solutionGeneric drugs (ANDA)May 13, 2016
Asclemed USA Inc.1injection, solutionOther unapproved drugsJanuary 24, 2026
Brookfield Pharmaceuticals, LLC.1injectionGeneric drugs (ANDA)October 31, 2022
Cardinal Health 107, LLC1injection, solutionGeneric drugs (ANDA)January 6, 2010
HF Acquisition Co LLC, DBA HealthFirst1injection, solutionGeneric drugs (ANDA)October 16, 2019
Huons Co., Ltd.1injectionGeneric drugs (ANDA)December 30, 2019

Dosage forms

Dosage formProductsShare
Injection, solution10198.1%
Injection21.9%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)8582.5%
New drug applications (NDA)1615.5%
Other unapproved drugs21.9%

Pharmacologic classes

ClassProducts
Amide Local Anesthetic103

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.