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Data / Drug companies / alpha-Glucosidase Inhibitor

alpha-Glucosidase Inhibitor drugs: 2 drugs from 9 companies in the FDA NDC directory

alpha-Glucosidase Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 23 products in this class from 9 companies, covering 2 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on April 16, 2021.

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.

  • 9Companies
  • 23Products
  • 2Drugs by generic name

Drugs in the alpha-Glucosidase Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Acarbose177
Miglitol62

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Chartwell RX, LLC3tabletGeneric drugs (ANDA)April 16, 2021
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)April 16, 2021
Hikma Pharmaceuticals USA Inc.3tabletGeneric drugs (ANDA)May 7, 2008
PD-Rx Pharmaceuticals, Inc.3tabletGeneric drugs (ANDA)May 7, 2008
Proficient Rx LP3tablet, coatedGeneric drugs (ANDA)January 15, 2021
Strides Pharma Science Limited3tabletGeneric drugs (ANDA)December 10, 2016
Westminster Pharmaceuticals, LLC3tablet, coatedGeneric drugs (ANDA)January 15, 2021
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)December 10, 2016
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)April 16, 2021

Dosage forms

Dosage formProductsShare
Tablet1773.9%
Tablet, coated626.1%

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.