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Data / Drug companies / Merz Pharmaceuticals, LLC

Merz Pharmaceuticals, LLC: 8 products in the FDA NDC directory, labeler code 0259

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

Merz Pharmaceuticals, LLC (labeler code 0259) lists 8 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 8 prescription drugs. Its main marketing category is biologics (BLA). The newest product started marketing on December 22, 2018.

The request: Watch Merz Pharmaceuticals, LLC (FDA labeler code 0259): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
0259
Products in commercial distribution
8
Packages
11
Finished drugs by generic name
4
Prescription products
8
Over the counter products
0
Flagged as original packager
8 of 8 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
March 1, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Biologics (BLA)562.5%
New drug applications (NDA)337.5%

Products by type

TypeProductsShare
Prescription drugs8100%

Drugs it lists

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

DrugProductsCompanies listing it
Incobotulinumtoxina52
Glycopyrrolate164
Levodopa12
Dalfampridine111

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution562.5%
Liquid112.5%
Capsule112.5%
Tablet, film coated, extended release112.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Inbrija0259-6142CapsuleNew drug applications (NDA)December 22, 2018
Xeomin0259-1620Injection, powder, lyophilized, for solutionBiologics (BLA)November 20, 2015
Cuvposa0259-0501LiquidNew drug applications (NDA)January 1, 2013
Xeomin0259-4150Injection, powder, lyophilized, for solutionBiologics (BLA)September 1, 2010
Xeomin0259-4110Injection, powder, lyophilized, for solutionBiologics (BLA)September 1, 2010
Xeomin0259-1610Injection, powder, lyophilized, for solutionBiologics (BLA)September 1, 2010
Xeomin0259-1605Injection, powder, lyophilized, for solutionBiologics (BLA)September 1, 2010
Ampyra0259-5010Tablet, film coated, extended releaseNew drug applications (NDA)March 1, 2010

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.