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Data / Drug companies / Dipharma Francis Srl

Dipharma Francis Srl: 72 products in the FDA NDC directory, labeler code 46438

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

Dipharma Francis Srl (labeler code 46438) lists 72 products in the FDA National Drug Code Directory. By type: 72 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on February 12, 2026.

The request: Watch Dipharma Francis Srl (FDA labeler code 46438): 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
46438
Products in commercial distribution
72
Packages
76
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule IV 3
Started marketing in the last 12 months
2
Earliest marketing start
January 7, 1980
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients72100%

Products by type

TypeProductsShare
Bulk ingredients72100%

Dosage forms

Dosage formProductsShare
Powder7097.2%
Liquid22.8%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sodium neridronate46438-0673PowderBulk ingredientsFebruary 12, 2026
Is5mn 90% lactose 200 10%46438-0672PowderBulk ingredientsFebruary 12, 2026
Migalastat hydrochloride46438-0674PowderBulk ingredientsJuly 29, 2025
Miglustat milled46438-0671PowderBulk ingredientsDecember 10, 2024
Miglustat46438-0665PowderBulk ingredientsDecember 10, 2024
Cholic acid46438-0669PowderBulk ingredientsNovember 28, 2024
Sapropterine dihydrochloride46438-0664PowderBulk ingredientsDecember 17, 2021
Nytroglycerin solution46438-0663LiquidBulk ingredientsMay 5, 2021
Rufinamide46438-0662PowderBulk ingredientsApril 15, 2021
Rufinamide46438-0661PowderBulk ingredientsApril 15, 2021
Sapropterin dihydrochloride46438-0660PowderBulk ingredientsDecember 11, 2020
Amitriptyline hydrochloride milled46438-0659PowderBulk ingredientsDecember 4, 2019
Chenodeoxycholic acid46438-0657PowderBulk ingredientsSeptember 1, 2019
Crisaborole46438-0656PowderBulk ingredientsJuly 9, 2019
Carglumic acid46438-0658PowderBulk ingredientsJuly 1, 2019
Modafinil46438-0655PowderBulk ingredientsAugust 1, 2018
Ursodiol46438-0653PowderBulk ingredientsAugust 1, 2018
Fexofenadine hydrochloride46438-0651PowderBulk ingredientsAugust 1, 2018
Tolbutamide46438-0650PowderBulk ingredientsAugust 1, 2018
Dapsone micronized46438-0649PowderBulk ingredientsAugust 1, 2018
7-ketolithocholic acid46438-0646PowderBulk ingredientsAugust 1, 2018
Dapsone46438-0645PowderBulk ingredientsAugust 1, 2018
Modafinil46438-0102PowderBulk ingredientsAugust 1, 2018
Tolbutamide46438-0002PowderBulk ingredientsAugust 1, 2018
Bupropion hydrochloride46438-0647PowderBulk ingredientsDecember 1, 2016

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.