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Data / Drug companies / Sterling Pharma Solutions Limited

Sterling Pharma Solutions Limited: 43 products in the FDA NDC directory, labeler code 50384

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

Sterling Pharma Solutions Limited (labeler code 50384) lists 43 products in the FDA National Drug Code Directory. By type: 42 bulk ingredients, 1 drugs for further processing. Its main marketing category is bulk ingredients. The newest product started marketing on July 24, 2026.

The request: Watch Sterling Pharma Solutions Limited (FDA labeler code 50384): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
50384
Products in commercial distribution
43
Packages
43
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 1
Started marketing in the last 12 months
1
Earliest marketing start
March 25, 1994
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients4093%
Bulk ingredients for compounding24.7%
Drugs for further processing12.3%

Products by type

TypeProductsShare
Bulk ingredients4297.7%
Drugs for further processing12.3%

Dosage forms

Dosage formProductsShare
Powder3990.7%
Suspension12.3%
Injection12.3%
Injection, solution12.3%
Liquid12.3%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Centanafadine hcl50384-0401PowderBulk ingredientsJuly 24, 2026
Avatrombopag maleate50384-0399PowderBulk ingredientsJune 9, 2025
Isoproterenol hydrochloride50384-0363PowderBulk ingredientsJune 9, 2025
Taurolidine50384-0235PowderBulk ingredientsNovember 15, 2023
Nilotinib hydrochloride50384-6700PowderBulk ingredientsJuly 3, 2023
Dabrafenib mesylate50384-6600PowderBulk ingredientsJuly 3, 2023
Capmatinib hydrochloride50384-6500PowderBulk ingredientsJuly 3, 2023
Octreotide acetate50384-6400PowderBulk ingredientsJuly 3, 2023
Ciclosporin50384-6300PowderBulk ingredientsJuly 3, 2023
Imatinib mesylate50384-6200PowderBulk ingredientsJuly 3, 2023
Valsartan50384-6100PowderBulk ingredientsJuly 3, 2023
Avatrombopag maleate50384-0340PowderBulk ingredientsDecember 6, 2022
Fuzapladib sodium50384-0287PowderBulk ingredientsNovember 14, 2022
Methylenediphosphonic acid50384-0425InjectionBulk ingredientsNovember 13, 2020
Oliceridine fumarate50384-0707Injection, solutionBulk ingredientsAugust 6, 2020
Tazemetostat hydrobromide50384-4000PowderBulk ingredientsJanuary 23, 2020
Diroximel fumarate50384-5015PowderBulk ingredientsOctober 30, 2019
Pexidartinib hcl50384-0750PowderBulk ingredients for compoundingAugust 5, 2019
Ferric maltol50384-5100PowderBulk ingredientsJuly 1, 2019
Sodium thiosulfate pentahydrate50384-0330PowderBulk ingredients for compoundingMay 1, 2019
Tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate50384-2804PowderBulk ingredientsJanuary 1, 2017
Deoxycholic acid50384-0151PowderBulk ingredientsApril 29, 2015
Grapiprant50384-0500PowderBulk ingredientsJanuary 1, 2015
Ractopamine hydrochloride50384-5060SuspensionDrugs for further processingJuly 16, 2013
Tetrakis(2-methoxy isobutyl isonitrile) copper(i) tetrafluoroborate50384-0700PowderBulk ingredientsJuly 10, 2009

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.