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Data / Drug companies / Hikal Limited

Hikal Limited: 35 products in the FDA NDC directory, labeler code 66651

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

Hikal Limited (labeler code 66651) lists 35 products in the FDA National Drug Code Directory. By type: 35 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on May 20, 2026.

The request: Watch Hikal Limited (FDA labeler code 66651): 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
66651
Products in commercial distribution
35
Packages
247
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule IV 1, Schedule V 2
Started marketing in the last 12 months
3
Earliest marketing start
January 12, 2015
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients35100%

Products by type

TypeProductsShare
Bulk ingredients35100%

Dosage forms

Dosage formProductsShare
Powder35100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Cariprazine hydrochloride66651-935PowderBulk ingredientsMay 20, 2026
Vonoprazan fumarate66651-934PowderBulk ingredientsMay 20, 2026
Bupropion hydrochloride66651-501PowderBulk ingredientsMay 12, 2026
Lubabegron fumarate66651-933PowderBulk ingredientsMarch 28, 2025
Edoxaban tosylate monohydrate66651-932PowderBulk ingredientsOctober 1, 2024
Celecoxib66651-502PowderBulk ingredientsSeptember 12, 2023
Rivaroxaban66651-503PowderBulk ingredientsAugust 18, 2023
Bupropion hydrobromide66651-930PowderBulk ingredientsJune 16, 2023
Bupropion hydrobromide66651-929PowderBulk ingredientsApril 10, 2023
Desvenlafaxine succinate66651-928PowderBulk ingredientsAugust 19, 2022
Vildagliptin66651-102PowderBulk ingredientsDecember 1, 2021
Sitagliptin phosphate anhydrate66651-925PowderBulk ingredientsOctober 19, 2020
Ertugliflozin66651-926PowderBulk ingredientsDecember 20, 2019
Dapagliflozin propanediol66651-924PowderBulk ingredientsDecember 20, 2019
Sitagliptin hydrochloride66651-923PowderBulk ingredientsSeptember 11, 2019
Pyrimethamine66651-922PowderBulk ingredientsDecember 15, 2017
Apixaban66651-921PowderBulk ingredientsDecember 12, 2017
Butorphanol tartrate66651-920PowderBulk ingredientsJuly 24, 2017
Celecoxib66651-919PowderBulk ingredientsJuly 24, 2017
Dabigatran etexilate mesylate66651-918PowderBulk ingredientsJuly 24, 2017
Sitagliptin phosphate66651-917PowderBulk ingredientsJuly 24, 2017
Valacyclovir hydrochloride66651-916PowderBulk ingredientsJuly 24, 2017
Pregabalin66651-915PowderBulk ingredientsJuly 24, 2017
Lacosamide66651-914PowderBulk ingredientsJuly 24, 2017
Pentoxifylline66651-912PowderBulk ingredientsAugust 18, 2015

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.