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Data / Drug companies / Edenbridge Pharmaceuticals LLC.

Edenbridge Pharmaceuticals LLC.: 37 products in the FDA NDC directory, labeler code 42799

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

Edenbridge Pharmaceuticals LLC. (labeler code 42799) lists 37 products in the FDA National Drug Code Directory, covering 23 finished drugs by generic name. By type: 37 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on June 3, 2026.

The request: Watch Edenbridge Pharmaceuticals LLC. (FDA labeler code 42799): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
42799
Products in commercial distribution
37
Packages
56
Finished drugs by generic name
23
Prescription products
37
Over the counter products
0
Controlled substance products
Schedule II 1
Flagged as original packager
37 of 37 products that carry the flag
Started marketing in the last 12 months
4
Products with a marketing end date set
2
Earliest marketing start
November 6, 2002
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)3183.8%
Other unapproved drugs38.1%
Authorized generics (NDA)38.1%

Products by type

TypeProductsShare
Prescription drugs37100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet1540.5%
Tablet, film coated616.2%
Capsule410.8%
Solution410.8%
Tablet, extended release410.8%
Solution/ drops12.7%
Tablet, film coated, extended release12.7%
Granule, delayed release12.7%
Tincture12.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tofacitinib42799-970Tablet, film coated, extended releaseGeneric drugs (ANDA)June 3, 2026
Atropine sulfate42799-826Solution/ dropsGeneric drugs (ANDA)May 6, 2026
Nintedanib42799-973CapsuleGeneric drugs (ANDA)April 3, 2026
Nintedanib42799-972CapsuleGeneric drugs (ANDA)April 3, 2026
Colestipol Hydrochloride42799-115TabletGeneric drugs (ANDA)November 26, 2024
Prednisolone Sodium Phosphate42799-815SolutionGeneric drugs (ANDA)October 9, 2023
Pantoprazole Sodium42799-952Granule, delayed releaseGeneric drugs (ANDA)June 16, 2023
Prednisolone Sodium Phosphate42799-816SolutionGeneric drugs (ANDA)May 1, 2023
Venlafaxine hydrochloride, extended release42799-963TabletGeneric drugs (ANDA)March 15, 2023
Venlafaxine hydrochloride, extended release42799-962TabletGeneric drugs (ANDA)March 15, 2023
Vigabatrin42799-950TabletGeneric drugs (ANDA)June 29, 2022
Loperamide Hydrochloride42799-605CapsuleGeneric drugs (ANDA)September 25, 2020
Yargesa42799-709CapsuleGeneric drugs (ANDA)August 6, 2020
Tinidazole42799-208TabletGeneric drugs (ANDA)December 20, 2019
Tinidazole42799-207TabletGeneric drugs (ANDA)December 20, 2019
Albendazole42799-110TabletGeneric drugs (ANDA)May 17, 2019
Bisoprolol Fumarate and Hydrochlorothiazide42799-922Tablet, film coatedGeneric drugs (ANDA)April 30, 2019
Bisoprolol Fumarate and Hydrochlorothiazide42799-921Tablet, film coatedGeneric drugs (ANDA)April 30, 2019
Bisoprolol Fumarate and Hydrochlorothiazide42799-920Tablet, film coatedGeneric drugs (ANDA)April 30, 2019
Etodolac42799-112Tablet, film coatedGeneric drugs (ANDA)December 7, 2018
Etodolac42799-111Tablet, film coatedGeneric drugs (ANDA)December 7, 2018
Isosorbide Mononitrate42799-960Tablet, extended releaseGeneric drugs (ANDA)November 15, 2018
Isosorbide Mononitrate42799-958Tablet, extended releaseGeneric drugs (ANDA)January 5, 2017
Ethacrynic Acid42799-405TabletGeneric drugs (ANDA)July 1, 2016
Donepezil hydrochloride42799-954Tablet, film coatedGeneric drugs (ANDA)February 19, 2016

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.