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Data / Drug companies / Tapi Hungary Industries Kft.

Tapi Hungary Industries Kft.: 21 products in the FDA NDC directory, labeler code 84671

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

Tapi Hungary Industries Kft. (labeler code 84671) lists 21 products in the FDA National Drug Code Directory. By type: 21 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on June 12, 2026.

The request: Watch Tapi Hungary Industries Kft. (FDA labeler code 84671): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
84671
Products in commercial distribution
21
Packages
21
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 1, Schedule IV 1
Started marketing in the last 12 months
1
Earliest marketing start
November 8, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients21100%

Products by type

TypeProductsShare
Bulk ingredients21100%

Dosage forms

Dosage formProductsShare
Powder21100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Oripavine84671-1062PowderBulk ingredientsJune 12, 2026
Fidaxomicin84671-1054PowderBulk ingredientsAugust 11, 2025
Pacritinib citrate84671-1061PowderBulk ingredientsApril 25, 2025
Pirtobrutinib84671-1060PowderBulk ingredientsApril 9, 2025
Trilaciclib hemi-citrate84671-1059PowderBulk ingredientsOctober 15, 2024
Deferoxamine mesylate84671-1016PowderBulk ingredientsJanuary 24, 2022
Mupirocin calcium84671-1046PowderBulk ingredientsApril 30, 2020
Pravastatin sodium84671-1022PowderBulk ingredientsApril 30, 2020
Midostaurin amorph84671-1058PowderBulk ingredientsNovember 14, 2019
Mupirocin84671-1017PowderBulk ingredientsAugust 21, 2019
Bicalutamide84671-1028PowderBulk ingredientsAugust 16, 2019
Lovastatin84671-1014PowderBulk ingredientsAugust 16, 2019
Ondansetron84671-1033PowderBulk ingredientsNovember 17, 2017
Zaleplon84671-1026PowderBulk ingredientsNovember 17, 2017
Ondansetron hydrochloride84671-1025PowderBulk ingredientsNovember 17, 2017
Tobramycin micronized84671-1041PowderBulk ingredientsOctober 30, 2017
Mycophenolate sodium84671-1049PowderBulk ingredientsJanuary 18, 2017
Simvastatin micronized84671-1042PowderBulk ingredientsApril 17, 2013
Tobramycin84671-1012PowderBulk ingredientsApril 10, 2013
Lovastatin84671-1040PowderBulk ingredientsJanuary 11, 2013
Imiquimod84671-1030PowderBulk ingredientsNovember 8, 2010

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.