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Data / Drug companies / Par Health USA, LLC

Par Health USA, LLC: 16 products in the FDA NDC directory, labeler code 0254

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

Par Health USA, LLC (labeler code 0254) lists 16 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 16 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on June 26, 2024.

The request: Watch Par Health USA, LLC (FDA labeler code 0254): 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
0254
Products in commercial distribution
16
Packages
16
Finished drugs by generic name
10
Prescription products
16
Over the counter products
0
Flagged as original packager
16 of 16 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
September 19, 2017
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1275%
Authorized generics (NDA)425%

Products by type

TypeProductsShare
Prescription drugs16100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule637.5%
Capsule, gelatin coated212.5%
Suspension212.5%
Tablet212.5%
Tablet, delayed release212.5%
Tablet, film coated16.2%
Tablet, coated16.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tiopronin0254-3035Tablet, delayed releaseGeneric drugs (ANDA)June 26, 2024
Tiopronin0254-3034Tablet, delayed releaseGeneric drugs (ANDA)June 26, 2024
Colchicine0254-0460CapsuleGeneric drugs (ANDA)November 1, 2023
Alvimopan0254-3012CapsuleGeneric drugs (ANDA)May 3, 2023
Posaconazole0254-1016SuspensionAuthorized generics (NDA)March 29, 2023
Chlorzoxazone0254-2053TabletGeneric drugs (ANDA)June 17, 2021
Lubiprostone0254-3029Capsule, gelatin coatedAuthorized generics (NDA)January 1, 2021
Lubiprostone0254-3028Capsule, gelatin coatedAuthorized generics (NDA)January 1, 2021
Chlorzoxazone0254-2005TabletGeneric drugs (ANDA)November 4, 2020
Diazoxide0254-1010SuspensionGeneric drugs (ANDA)July 21, 2020
Penicillamine0254-2000Tablet, film coatedGeneric drugs (ANDA)January 2, 2020
Nitisinone0254-3022CapsuleGeneric drugs (ANDA)October 4, 2019
Nitisinone0254-3021CapsuleGeneric drugs (ANDA)October 4, 2019
Nitisinone0254-3020CapsuleGeneric drugs (ANDA)October 4, 2019
Posaconazole0254-2045Tablet, coatedAuthorized generics (NDA)August 30, 2019
Omega-3-acid ethyl esters0254-3010CapsuleGeneric drugs (ANDA)September 19, 2017

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.