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Data / Drug companies / Porton Pharma Solutions Ltd

Porton Pharma Solutions Ltd: 11 products in the FDA NDC directory, labeler code 75877

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

Porton Pharma Solutions Ltd (labeler code 75877) lists 11 products in the FDA National Drug Code Directory. By type: 11 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on July 8, 2026.

The request: Watch Porton Pharma Solutions Ltd (FDA labeler code 75877): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
75877
Products in commercial distribution
11
Packages
18
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
3
Earliest marketing start
February 27, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients11100%

Products by type

TypeProductsShare
Bulk ingredients11100%

Dosage forms

Dosage formProductsShare
Powder11100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Abemaciclib75877-0011PowderBulk ingredientsJuly 8, 2026
Ribociclib succinate75877-0010PowderBulk ingredientsMay 13, 2026
Orforglipron hemicalcium hydrate75877-0009PowderBulk ingredientsMay 1, 2026
Vibegron75877-0008PowderBulk ingredientsMay 27, 2023
Vibegron75877-0008PowderBulk ingredientsMay 27, 2023
Darunavir ethanolate75877-0007PowderBulk ingredientsMarch 26, 2019
Mefloquine hcl micronized75877-0006PowderBulk ingredientsNovember 28, 2017
Mefloquine hcl75877-0005PowderBulk ingredientsNovember 28, 2017
Tiopronin75877-0004PowderBulk ingredientsJanuary 10, 2014
Propofol75877-0003PowderBulk ingredientsJune 1, 2013
Nicotine75877-0002PowderBulk ingredientsFebruary 27, 2012

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.