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Data / Drug companies / TruPharma, LLC

TruPharma, LLC: 85 products in the FDA NDC directory, labeler code 52817

TruPharma, LLC (labeler code 52817) lists 85 products in the FDA National Drug Code Directory, covering 40 finished drugs by generic name. By type: 85 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on October 16, 2026.

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
52817
Products in commercial distribution
85
Packages
136
Finished drugs by generic name
40
Prescription products
85
Over the counter products
0
Controlled substance products
Schedule IV 7
Flagged as original packager
68 of 68 products that carry the flag
Started marketing in the last 12 months
14
Products with a marketing end date set
3
Earliest marketing start
August 1, 2016
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)7487.1%
Authorized generics (NDA)910.6%
Other unapproved drugs11.2%
New drug applications (NDA)11.2%

Products by type

TypeProductsShare
Prescription drugs85100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet2934.1%
Tablet, film coated2023.5%
Solution910.6%
Patch67.1%
Capsule55.9%
Tablet, coated22.4%
Cream22.4%
Powder, for solution22.4%
Tablet, delayed release22.4%
Ointment22.4%
Suspension22.4%
Gel22.4%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sertraline Hydrochloride52817-224Tablet, film coatedGeneric drugs (ANDA)October 16, 2026
Sertraline Hydrochloride52817-223Tablet, film coatedGeneric drugs (ANDA)October 16, 2026
Trazodone Hydrochloride52817-396Tablet, film coatedGeneric drugs (ANDA)September 3, 2026
Trazodone Hydrochloride52817-395Tablet, film coatedGeneric drugs (ANDA)September 3, 2026
Clonazepam52817-305TabletGeneric drugs (ANDA)September 1, 2026
Prednisolone52817-860SolutionGeneric drugs (ANDA)August 4, 2026
Oxybutynin Chloride52817-261TabletGeneric drugs (ANDA)July 28, 2026
Cyproheptadine Hydrochloride52817-415TabletGeneric drugs (ANDA)June 1, 2026
Clonidine hydrochloride52817-183TabletGeneric drugs (ANDA)April 13, 2026
Clonidine Transdermal System USP, 0.3 mg/day52817-507PatchAuthorized generics (NDA)March 30, 2026
Clonidine Transdermal System USP, 0.2 mg/day52817-506PatchAuthorized generics (NDA)March 30, 2026
Clonidine Transdermal System USP, 0.1 mg/day52817-505PatchAuthorized generics (NDA)March 30, 2026
Sapropterin Dihydrochloride52817-851Powder, for solutionGeneric drugs (ANDA)January 30, 2026
Sapropterin Dihydrochloride52817-850Powder, for solutionGeneric drugs (ANDA)January 30, 2026
Bisoprolol Fumarate52817-268Tablet, film coatedGeneric drugs (ANDA)March 7, 2025
Nitroglycerin52817-835OintmentGeneric drugs (ANDA)December 2, 2024
Dapsone52817-832GelGeneric drugs (ANDA)November 20, 2024
Sucralfate52817-840SuspensionGeneric drugs (ANDA)April 1, 2024
Dapsone52817-831GelGeneric drugs (ANDA)March 1, 2024
Baclofen52817-318TabletGeneric drugs (ANDA)February 5, 2024
Metoprolol tartrate52817-254TabletGeneric drugs (ANDA)January 17, 2024
Metoprolol tartrate52817-253TabletGeneric drugs (ANDA)January 17, 2024
Metoprolol tartrate52817-252TabletGeneric drugs (ANDA)January 17, 2024
Metoprolol tartrate52817-251TabletGeneric drugs (ANDA)January 17, 2024
Metoprolol tartrate52817-250TabletGeneric drugs (ANDA)January 17, 2024

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.