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Data / Drug companies / Symed Labs Limited

Symed Labs Limited: 37 products in the FDA NDC directory, labeler code 66022

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

Symed Labs Limited (labeler code 66022) lists 37 products in the FDA National Drug Code Directory. By type: 37 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on January 1, 2026.

The request: Watch Symed Labs Limited (FDA labeler code 66022): 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
66022
Products in commercial distribution
37
Packages
39
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule III 3, Schedule IV 4
Started marketing in the last 12 months
1
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 ingredients37100%

Products by type

TypeProductsShare
Bulk ingredients37100%

Dosage forms

Dosage formProductsShare
Powder37100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Flibanserin66022-0123PowderBulk ingredientsJanuary 1, 2026
Otilonium bromide66022-0305PowderBulk ingredientsJune 28, 2024
Bilastine (form-i)66022-0213PowderBulk ingredientsJune 28, 2024
Ezetimibe66022-0212PowderBulk ingredientsDecember 13, 2023
Modafinil66022-0208PowderBulk ingredientsOctober 14, 2023
Vortioxetine hydrobromide66022-0211PowderBulk ingredientsSeptember 30, 2023
Bilastine (form-ii)66022-0210PowderBulk ingredientsSeptember 30, 2023
Hydroxychloroquine sulfate66022-0209PowderBulk ingredientsSeptember 30, 2023
Hydroxyzine pamoate66022-0122PowderBulk ingredientsJune 23, 2023
Sertraline hydrochloride66022-0304PowderBulk ingredientsOctober 4, 2021
Prucalopride succinate66022-0207PowderBulk ingredientsDecember 14, 2018
Deferasirox66022-0301PowderBulk ingredientsMay 18, 2017
Sucroferric oxyhydroxide66022-0302PowderBulk ingredientsNovember 27, 2013
Brimonidine tartrate66022-0110PowderBulk ingredientsAugust 23, 2013
Carbinoxamine maleate66022-0121PowderBulk ingredientsMarch 28, 2013
Rivaroxaban66022-0203PowderBulk ingredientsJuly 1, 2011
Dronedarone hydrochloride66022-0118PowderBulk ingredientsJuly 1, 2009
Iloperidone66022-0115PowderBulk ingredientsMay 6, 2009
Meprobamate66022-0105PowderBulk ingredientsFebruary 27, 2008
Levocetirizine dihydrochloride66022-0108PowderBulk ingredientsJanuary 28, 2008
Levocetirizine dihydrochloride66022-0108PowderBulk ingredientsJanuary 28, 2008
Iron sucrose66022-0119PowderBulk ingredientsMarch 20, 2005
Eszopiclone66022-0106PowderBulk ingredientsDecember 15, 2004
Lanthanum carbonate66022-0116PowderBulk ingredientsOctober 16, 2004
Linezolid66022-0201PowderBulk ingredientsApril 18, 2000

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.