Skip to the page

Data / Drug companies / F.i.s. Fabbrica Italiana Sintetici S.p.a.

F.i.s. Fabbrica Italiana Sintetici S.p.a.: 14 products in the FDA NDC directory, labeler code 52133

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

F.i.s. Fabbrica Italiana Sintetici S.p.a. (labeler code 52133) lists 14 products in the FDA National Drug Code Directory. By type: 14 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on October 3, 2013.

The request: Watch F.i.s. Fabbrica Italiana Sintetici S.p.a. (FDA labeler code 52133): 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
52133
Products in commercial distribution
14
Packages
14
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
January 1, 1982
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients14100%

Products by type

TypeProductsShare
Bulk ingredients14100%

Dosage forms

Dosage formProductsShare
Powder1392.9%
Liquid17.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tse-424 acetate52133-0032PowderBulk ingredientsOctober 3, 2013
Fosaprepitant dimeglumine52133-0045PowderBulk ingredientsNovember 12, 2010
Nebivolol hydrochloride52133-0039PowderBulk ingredientsDecember 17, 2007
Fosfomycin trometamol52133-0018PowderBulk ingredientsDecember 19, 1996
Olopatadine hydrochloride52133-0036PowderBulk ingredientsDecember 18, 1996
Propofol52133-0023LiquidBulk ingredientsJune 11, 1996
Dorzolamide hydrochloride52133-0031PowderBulk ingredientsDecember 9, 1994
Dorzolamide hydrochloride52133-0031PowderBulk ingredientsDecember 9, 1994
Gabapentin52133-0025PowderBulk ingredientsDecember 30, 1992
Diltiazem hydrochloride52133-0013PowderBulk ingredientsAugust 10, 1992
Nifedipine52133-0028PowderBulk ingredientsNovember 27, 1985
Nifedipine52133-0009PowderBulk ingredientsJanuary 1, 1982
Sulindac52133-0007PowderBulk ingredientsJanuary 1, 1982
Acetylcysteine52133-0002PowderBulk ingredientsJanuary 1, 1982

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.