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Data / Drug companies / Coral Way Pharma, LLC

Coral Way Pharma, LLC: 5 products in the FDA NDC directory, labeler code 85437

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

Coral Way Pharma, LLC (labeler code 85437) lists 5 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 5 prescription drugs. Its main marketing category is authorized generics (NDA). The newest product started marketing on October 4, 2026.

The request: Watch Coral Way Pharma, LLC (FDA labeler code 85437): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
85437
Products in commercial distribution
5
Packages
5
Finished drugs by generic name
5
Prescription products
5
Over the counter products
0
Flagged as original packager
4 of 4 products that carry the flag
Started marketing in the last 12 months
4
Products with a marketing end date set
1
Earliest marketing start
October 29, 2025
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Authorized generics (NDA)240%
Generic drugs (ANDA)240%
New drug applications (NDA)120%

Products by type

TypeProductsShare
Prescription drugs5100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule240%
Cream120%
Tablet, film coated120%
Lotion120%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Cyclobenzaprine hydrochloride85437-013Tablet, film coatedGeneric drugs (ANDA)October 4, 2026
Fenoprofen Calcium85437-502CapsuleGeneric drugs (ANDA)July 15, 2026
Halobetasol Propionate85437-008LotionAuthorized generics (NDA)March 10, 2026
Ertaczo85437-004CreamNew drug applications (NDA)November 7, 2025
Auranofin85437-093CapsuleAuthorized generics (NDA)October 29, 2025

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.