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Data / Drug companies / Pfizer Ireland Pharmaceuticals Unlimited Company

Pfizer Ireland Pharmaceuticals Unlimited Company: 21 products in the FDA NDC directory, labeler code 60715

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

Pfizer Ireland Pharmaceuticals Unlimited Company (labeler code 60715) lists 21 products in the FDA National Drug Code Directory. By type: 21 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on March 13, 2024.

The request: Watch Pfizer Ireland Pharmaceuticals Unlimited Company (FDA labeler code 60715): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
60715
Products in commercial distribution
21
Packages
22
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
January 29, 1990
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients21100%

Products by type

TypeProductsShare
Bulk ingredients21100%

Dosage forms

Dosage formProductsShare
Powder21100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Etrasimod60715-0274PowderBulk ingredientsMarch 13, 2024
Crizotinib60715-1551PowderBulk ingredientsOctober 27, 2023
Talazoparib tosylate60715-2345PowderBulk ingredientsJanuary 9, 2023
Nirmatrelvir60715-2085PowderBulk ingredientsAugust 19, 2022
Crisaborole60715-3211PowderBulk ingredientsOctober 8, 2020
Prazosin hydrochloride60715-0011PowderBulk ingredientsSeptember 1, 2020
Voriconazole60715-1700PowderBulk ingredientsJanuary 1, 2019
Tafamidis60715-4344PowderBulk ingredientsOctober 31, 2018
Tafamidis60715-0647PowderBulk ingredientsOctober 31, 2018
Tigecycline60715-1001PowderBulk ingredientsJune 19, 2018
Ziprasidone mesilate60715-1203PowderBulk ingredientsMarch 26, 2018
Temsirolimus60715-1125PowderBulk ingredientsFebruary 1, 2017
Dacomitinib60715-0015PowderBulk ingredientsNovember 7, 2016
Doxycycline hyclate60715-0445PowderBulk ingredientsApril 2, 2014
Palbociclib60715-0188PowderBulk ingredientsOctober 4, 2013
Tofacitinib citrate60715-1000PowderBulk ingredientsNovember 6, 2012
Azithromycin60715-3150PowderBulk ingredientsDecember 29, 2011
Dofetilide60715-2811PowderBulk ingredientsFebruary 25, 2011
Fesoterodine fumarate60715-0242PowderBulk ingredientsJanuary 1, 2008
Piroxicam60715-3270PowderBulk ingredientsFebruary 13, 2003
Fluconazole60715-0020PowderBulk ingredientsJanuary 29, 1990

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.