Skip to the page

Data / Drug companies / Siegfried AG

Siegfried AG: 24 products in the FDA NDC directory, labeler code 17205

Siegfried AG (labeler code 17205) lists 24 products in the FDA National Drug Code Directory. By type: 22 bulk ingredients, 2 drugs for further processing. Its main marketing category is bulk ingredients. The newest product started marketing on April 18, 2024.

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
17205
Products in commercial distribution
24
Packages
24
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule III 2, Schedule V 1
Started marketing in the last 12 months
0
Earliest marketing start
December 7, 1973
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients2187.5%
Drugs for further processing28.3%
Bulk ingredients for compounding14.2%

Products by type

TypeProductsShare
Bulk ingredients2291.7%
Drugs for further processing28.3%

Dosage forms

Dosage formProductsShare
Powder2395.8%
Liquid14.2%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Venlafaxine hcl17205-567PowderBulk ingredientsApril 18, 2024
Lotilaner17205-629PowderBulk ingredientsAugust 14, 2023
Zanubrutinib17205-628PowderDrugs for further processingJune 16, 2023
Thalidomide17205-205PowderDrugs for further processingApril 1, 2023
Primidone17205-308PowderBulk ingredientsJune 30, 2020
Oclacitinib maleate17205-097PowderBulk ingredientsApril 12, 2019
Sarolaner17205-099PowderBulk ingredientsJanuary 31, 2019
Pimavanserin tartrate17205-098PowderBulk ingredientsApril 29, 2016
Nicotine polacrilex17205-483PowderBulk ingredientsDecember 12, 2012
Lacosamide17205-107PowderBulk ingredientsApril 20, 2010
Naltrexone base17205-102PowderBulk ingredientsApril 14, 2010
Naloxone hydrochloride17205-101PowderBulk ingredientsMarch 1, 2010
Buprenorphine base17205-100PowderBulk ingredientsJanuary 27, 2010
Naltrexone hydrochloride17205-108PowderBulk ingredients for compoundingJanuary 1, 2010
Naltrexone hydrochloride17205-103PowderBulk ingredientsJanuary 1, 2010
Fluoxetine hcl17205-612PowderBulk ingredientsJuly 2, 2008
Buprenorphine hcl17205-482PowderBulk ingredientsNovember 12, 2007
Nicotine bitartrate dihydrate17205-105PowderBulk ingredientsMarch 9, 2004
Topiramate17205-096PowderBulk ingredientsDecember 24, 1996
Proparacaine hydrochloride17205-340PowderBulk ingredientsJune 21, 1996
Nicotine17205-601LiquidBulk ingredientsNovember 18, 1988
Oxiconazole nitrate17205-104PowderBulk ingredientsOctober 22, 1984
Trimethobenzamide hcl17205-416PowderBulk ingredientsFebruary 27, 1981
Primidone17205-307PowderBulk ingredientsDecember 7, 1973

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