Skip to the page

Data / Drug companies / Sigmapharm Laboratories, LLC

Sigmapharm Laboratories, LLC: 27 products in the FDA NDC directory, labeler code 42794

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

Sigmapharm Laboratories, LLC (labeler code 42794) lists 27 products in the FDA National Drug Code Directory, covering 12 finished drugs by generic name. By type: 27 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on November 21, 2025.

The request: Watch Sigmapharm Laboratories, LLC (FDA labeler code 42794): each new product listing and each discontinued product. $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.

Labeler code
42794
Products in commercial distribution
27
Packages
50
Finished drugs by generic name
12
Prescription products
27
Over the counter products
0
Flagged as original packager
27 of 27 products that carry the flag
Started marketing in the last 12 months
3
Earliest marketing start
November 15, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)27100%

Products by type

TypeProductsShare
Prescription drugs27100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Tablet1555.6%
Capsule829.6%
Tablet, film coated414.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Liomny42794-133TabletGeneric drugs (ANDA)November 21, 2025
Liomny42794-132TabletGeneric drugs (ANDA)November 21, 2025
Liomny42794-131TabletGeneric drugs (ANDA)November 21, 2025
Disulfiram42794-029TabletGeneric drugs (ANDA)January 11, 2022
Disulfiram42794-028TabletGeneric drugs (ANDA)November 1, 2021
Amiloride Hydrochloride42794-005TabletGeneric drugs (ANDA)June 14, 2021
Asenapine42794-017TabletGeneric drugs (ANDA)December 14, 2020
Asenapine42794-016TabletGeneric drugs (ANDA)December 14, 2020
Protriptyline Hydrochloride42794-007Tablet, film coatedGeneric drugs (ANDA)March 2, 2020
Protriptyline Hydrochloride42794-004Tablet, film coatedGeneric drugs (ANDA)March 2, 2020
Ambrisentan42794-052Tablet, film coatedGeneric drugs (ANDA)April 10, 2019
Ambrisentan42794-051Tablet, film coatedGeneric drugs (ANDA)April 10, 2019
Dofetilide42794-046CapsuleGeneric drugs (ANDA)June 11, 2018
Dofetilide42794-045CapsuleGeneric drugs (ANDA)June 11, 2018
Dofetilide42794-044CapsuleGeneric drugs (ANDA)June 11, 2018
Flucytosine42794-010CapsuleGeneric drugs (ANDA)June 1, 2018
Flucytosine42794-009CapsuleGeneric drugs (ANDA)June 1, 2018
Acitretin42794-083CapsuleGeneric drugs (ANDA)September 16, 2015
Acitretin42794-081CapsuleGeneric drugs (ANDA)September 16, 2015
Acitretin42794-080CapsuleGeneric drugs (ANDA)September 16, 2015
Adefovir dipivoxil42794-003TabletGeneric drugs (ANDA)September 3, 2013
Griseofulvin42794-012TabletGeneric drugs (ANDA)December 6, 2012
Liothyronine Sodium42794-020TabletGeneric drugs (ANDA)December 3, 2012
Liothyronine Sodium42794-019TabletGeneric drugs (ANDA)December 3, 2012
Liothyronine Sodium42794-018TabletGeneric drugs (ANDA)December 3, 2012

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.