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Data / Drug companies / Pfizer Asia Manufacturing Pte Ltd

Pfizer Asia Manufacturing Pte Ltd: 11 products in the FDA NDC directory, labeler code 68724

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

Pfizer Asia Manufacturing Pte Ltd (labeler code 68724) 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 November 15, 2023.

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Labeler code
68724
Products in commercial distribution
11
Packages
14
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule V 1
Started marketing in the last 12 months
0
Earliest marketing start
October 2, 1998
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
Palbociclib68724-0187PowderBulk ingredientsNovember 15, 2023
Tafamidis68724-8730PowderBulk ingredientsApril 4, 2021
Tofacitinib citrate68724-1000PowderBulk ingredientsJanuary 12, 2019
Crizotinib68724-1020PowderBulk ingredientsAugust 29, 2018
Pregabalin68724-1235PowderBulk ingredientsOctober 7, 2017
Exemestane68724-1003PowderBulk ingredientsDecember 16, 2016
Doxasosin mesylate68724-1001PowderBulk ingredientsAugust 26, 2016
Azithromycin dihydrate68724-2124PowderBulk ingredientsJuly 3, 2014
Sunitinib malate68724-1234PowderBulk ingredientsDecember 21, 2013
Linezolid68724-5135PowderBulk ingredientsMay 20, 2009
Celecoxib68724-1004PowderBulk ingredientsOctober 2, 1998

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.