Skip to the page

Data / Drug companies / Alivus Life Sciences Limited

Alivus Life Sciences Limited: 109 products in the FDA NDC directory, labeler code 66039

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

Alivus Life Sciences Limited (labeler code 66039) lists 109 products in the FDA National Drug Code Directory. By type: 109 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on August 10, 2026.

The request: Watch Alivus Life Sciences Limited (FDA labeler code 66039): 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
66039
Products in commercial distribution
109
Packages
109
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule IV 4, Schedule V 3
Started marketing in the last 12 months
2
Earliest marketing start
October 2, 2003
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients109100%

Products by type

TypeProductsShare
Bulk ingredients109100%

Dosage forms

Dosage formProductsShare
Powder109100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Azelaic acid66039-985PowderBulk ingredientsAugust 10, 2026
Viloxazine hydrochloride66039-980PowderBulk ingredientsDecember 23, 2025
Bupropion hydrobromide66039-863PowderBulk ingredientsMarch 29, 2025
Ruxolitinib phosphate66039-976PowderBulk ingredientsMarch 27, 2025
Relugolix66039-974PowderBulk ingredientsMarch 26, 2025
Raloxifene hydrochloride66039-961PowderBulk ingredientsMarch 25, 2025
Finerenone66039-975PowderBulk ingredientsMarch 24, 2025
Tivozanib hydrochloride monohydrate66039-973PowderBulk ingredientsDecember 16, 2024
Fluvoxamine maleate66039-971PowderBulk ingredientsJuly 1, 2024
Propranolol hydrochloride66039-972PowderBulk ingredientsMarch 29, 2024
Sodium bicarbonate66039-970PowderBulk ingredientsMarch 28, 2024
Roflumilast66039-964PowderBulk ingredientsMarch 28, 2024
Brivaracetam66039-967PowderBulk ingredientsNovember 6, 2023
Trazodone hydrochloride66039-965PowderBulk ingredientsSeptember 29, 2023
Olaparib66039-968PowderBulk ingredientsSeptember 28, 2023
Isavuconazonium sulfate66039-963PowderBulk ingredientsNovember 30, 2022
Labetalol hydrochloride66039-962PowderBulk ingredientsAugust 8, 2022
Tafamidis66039-960PowderBulk ingredientsFebruary 10, 2022
Tafamidis meglumine66039-959PowderBulk ingredientsFebruary 10, 2022
Hydralazine hydrochloride66039-957PowderBulk ingredientsFebruary 24, 2021
Verapamil hydrochloride66039-956PowderBulk ingredientsNovember 28, 2020
Rosuvastatin calcium66039-955PowderBulk ingredientsOctober 27, 2020
Solriamfetol hydrochloride66039-953PowderBulk ingredientsSeptember 8, 2020
Iron sucrose66039-954PowderBulk ingredientsJuly 31, 2020
Lifitegrast66039-948PowderBulk ingredientsAugust 29, 2019

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.