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Data / Drug companies / Quimica Sintetica S.A.

Quimica Sintetica S.A.: 58 products in the FDA NDC directory, labeler code 53069

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

Quimica Sintetica S.A. (labeler code 53069) lists 58 products in the FDA National Drug Code Directory. By type: 58 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on April 17, 2026.

The request: Watch Quimica Sintetica S.A. (FDA labeler code 53069): 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
53069
Products in commercial distribution
58
Packages
58
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule IV 1
Started marketing in the last 12 months
4
Earliest marketing start
March 5, 1990
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients58100%

Products by type

TypeProductsShare
Bulk ingredients58100%

Dosage forms

Dosage formProductsShare
Powder58100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Bumetanide53069-1190PowderBulk ingredientsApril 17, 2026
Eltrombopag olamine53069-1180PowderBulk ingredientsApril 17, 2026
Eltrombopag olamine53069-1170PowderBulk ingredientsApril 17, 2026
Bumetanide micronized53069-1160PowderBulk ingredientsApril 17, 2026
Guanfacine53069-1150PowderBulk ingredientsSeptember 24, 2024
Spinosad53069-1130PowderBulk ingredientsSeptember 16, 2024
Zopiclone53069-1140PowderBulk ingredientsSeptember 6, 2024
Rivaroxaban53069-1120PowderBulk ingredientsJanuary 19, 2024
Rivaroxaban53069-1110PowderBulk ingredientsJanuary 19, 2024
Abiraterone acetate53069-1030PowderBulk ingredientsMay 22, 2018
Rabeprazole sodium53069-0980PowderBulk ingredientsDecember 21, 2017
Isradipine53069-0630PowderBulk ingredientsDecember 21, 2017
Ketorolac tromethamine53069-0620PowderBulk ingredientsDecember 21, 2017
Edaravone53069-1070PowderBulk ingredientsMay 5, 2017
Ciprofloxacin hydrochloride compacted53069-0690PowderBulk ingredientsFebruary 21, 2017
Apremilast53069-1050PowderBulk ingredientsMarch 21, 2014
Apremilast53069-1040PowderBulk ingredientsMarch 21, 2014
Droxidopa53069-1060PowderBulk ingredientsFebruary 18, 2014
Levomilnacipran hydrochloride53069-1100PowderBulk ingredientsJuly 25, 2013
Levomilnacipran hydrochloride53069-1090PowderBulk ingredientsJuly 25, 2013
Besifloxacin hydrochloride53069-1010PowderBulk ingredientsMay 28, 2009
Tianeptine sodium53069-0940PowderBulk ingredientsDecember 12, 2008
Meloxicam53069-0790PowderBulk ingredientsNovember 24, 2005
Rabeprazole sodium53069-0650PowderBulk ingredientsJanuary 1, 2005
Terbinafine hydrochloride53069-0530PowderBulk ingredientsDecember 14, 2004

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.