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Data / Drug companies / Polarean, Inc.

Polarean, Inc.: 5 products in the FDA NDC directory, labeler code 80534

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

Polarean, Inc. (labeler code 80534) lists 5 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 5 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on December 23, 2022.

The request: Watch Polarean, Inc. (FDA labeler code 80534): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
80534
Products in commercial distribution
5
Packages
6
Finished drugs by generic name
1
Prescription products
5
Over the counter products
0
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
December 23, 2022
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)5100%

Products by type

TypeProductsShare
Prescription drugs5100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Xenon xe 129 hyperpolarized51

Dosage forms

Dosage formProductsShare
Gas5100%

Pharmacologic classes

FDA established pharmacologic classes of its products.

ClassProducts
Hyperpolarized Contrast Agent4

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Xenoview80534-6350GasNew drug applications (NDA)December 23, 2022
Xenoview80534-1000GasNew drug applications (NDA)December 23, 2022
Xenoview80534-0750GasNew drug applications (NDA)December 23, 2022
Xenoview80534-0500GasNew drug applications (NDA)December 23, 2022
Xenoview80534-0300GasNew drug applications (NDA)December 23, 2022

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.