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Data / Drug companies / Viyash Scientific Limited

Viyash Scientific Limited: 84 products in the FDA NDC directory, labeler code 87832

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

Viyash Scientific Limited (labeler code 87832) lists 84 products in the FDA National Drug Code Directory. By type: 84 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on July 1, 2026.

The request: Watch Viyash Scientific Limited (FDA labeler code 87832): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
87832
Products in commercial distribution
84
Packages
84
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 1, Schedule III 1, Schedule IV 4, Schedule V 1
Started marketing in the last 12 months
1
Earliest marketing start
July 1, 2020
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients84100%

Products by type

TypeProductsShare
Bulk ingredients84100%

Dosage forms

Dosage formProductsShare
Powder8297.6%
Injection, powder, for solution11.2%
Poultice11.2%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ezetimibe87832-0311PowderBulk ingredientsJuly 1, 2026
Flibanserin87832-0517PowderBulk ingredientsJuly 1, 2021
Hydroxyzine pamoate87832-0516PowderBulk ingredientsJuly 1, 2021
Carbinoxamine maleate87832-0515PowderBulk ingredientsJuly 1, 2021
Carvedilol87832-0514PowderBulk ingredientsJuly 1, 2021
Iron sucrose87832-0513PowderBulk ingredientsJuly 1, 2021
Dronedarone hydrochloride87832-0512PowderBulk ingredientsJuly 1, 2021
Ketorolac tromethamine87832-0511PowderBulk ingredientsJuly 1, 2021
Lanthanum carbonate87832-0510PowderBulk ingredientsJuly 1, 2021
Iloperidone87832-0509PowderBulk ingredientsJuly 1, 2021
Meclizine hydrochloride87832-0508PowderBulk ingredientsJuly 1, 2021
Phentermine hydrochloride87832-0507PowderBulk ingredientsJuly 1, 2021
Brimonidine tartrate87832-0506PowderBulk ingredientsJuly 1, 2021
Levocetirizine dihydrochloride87832-0505PowderBulk ingredientsJuly 1, 2021
Eszopiclone87832-0504PowderBulk ingredientsJuly 1, 2021
Meprobamate87832-0503PowderBulk ingredientsJuly 1, 2021
Hydroxyzine hydrochloride87832-0502PowderBulk ingredientsJuly 1, 2021
Linezolid(form-iii)87832-0501PowderBulk ingredientsJuly 1, 2021
Sertraline hydrochloride (form-i)87832-0405PowderBulk ingredientsJuly 1, 2021
Otilonium bromide87832-0404PowderBulk ingredientsJuly 1, 2021
Hydroxyzine hydrochloride87832-0403PowderBulk ingredientsJuly 1, 2021
Sucroferric oxyhydroxide87832-0402PowderBulk ingredientsJuly 1, 2021
Deferasirox87832-0401PowderBulk ingredientsJuly 1, 2021
Vibegron87832-0225PoulticeBulk ingredientsJuly 1, 2021
Lisdexamfetamine dimesylate87832-0224PowderBulk ingredientsJuly 1, 2021

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.