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Data / Drug companies / Czech-Gen, A.s.

Czech-Gen, A.s.: 11 products in the FDA NDC directory, labeler code 63278

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

Czech-Gen, A.s. (labeler code 63278) lists 11 products in the FDA National Drug Code Directory. By type: 11 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on February 21, 2017.

The request: Watch Czech-Gen, A.s. (FDA labeler code 63278): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
63278
Products in commercial distribution
11
Packages
18
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule IV 3
Started marketing in the last 12 months
0
Earliest marketing start
January 1, 1983
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients11100%

Products by type

TypeProductsShare
Bulk ingredients11100%

Dosage forms

Dosage formProductsShare
Powder11100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Regadenoson monohydrate63278-1068PowderBulk ingredientsFebruary 21, 2017
Zolpidem tartrate63278-0490PowderBulk ingredientsJanuary 1, 2006
Zopiclone63278-1060PowderBulk ingredientsJanuary 1, 2005
Eszopiclone63278-1059PowderBulk ingredientsJanuary 1, 2005
Alfuzosin hydrochloride63278-0500PowderBulk ingredientsJanuary 1, 2004
Tizanidine hydrochloride63278-0489PowderBulk ingredientsJanuary 1, 2003
Brimonidine tartrate63278-0488PowderBulk ingredientsJanuary 1, 2002
Dofetilide63278-1079PowderBulk ingredientsOctober 1, 2000
Selegiline hydrochloride63278-0102PowderBulk ingredientsJanuary 1, 1997
Riluzole63278-1076PowderBulk ingredientsDecember 22, 1996
Warfarin sodium63278-1058PowderBulk ingredientsJanuary 1, 1983

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.