Skip to the page

Data / Drug companies / Synthimed Labs Private Limited

Synthimed Labs Private Limited: 14 products in the FDA NDC directory, labeler code 65096

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

Synthimed Labs Private Limited (labeler code 65096) 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 August 31, 2018.

The request: Watch Synthimed Labs Private Limited (FDA labeler code 65096): 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
65096
Products in commercial distribution
14
Packages
54
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, 2004
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
Powder14100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Letrozole65096-0116PowderBulk ingredientsAugust 31, 2018
Ropinirole hydrochloride65096-0102PowderBulk ingredientsJuly 12, 2013
Anastrozole65096-0117PowderBulk ingredientsDecember 1, 2010
Cinacalcet hydrochloride65096-0114PowderBulk ingredientsDecember 1, 2010
Ezetimibe65096-0113PowderBulk ingredientsDecember 1, 2010
Acamprosate calcium65096-0112PowderBulk ingredientsDecember 1, 2010
Donepezil hydrochloride65096-0109PowderBulk ingredientsDecember 1, 2010
Nateglinide65096-0108PowderBulk ingredientsDecember 1, 2010
Fexofenadine hydrochloride65096-0103PowderBulk ingredientsDecember 1, 2010
Risedronate sodium65096-0110PowderBulk ingredientsNovember 1, 2010
Aripiprazole65096-0107PowderBulk ingredientsMay 1, 2010
Pioglitazone hydrochloride65096-0104PowderBulk ingredientsJanuary 1, 2008
Quetiapine fumarate65096-0106PowderBulk ingredientsJanuary 1, 2007
Clarithromycin65096-0100PowderBulk ingredientsJanuary 1, 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.