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Data / Drug companies / Teva Neuroscience, Inc.

Teva Neuroscience, Inc.: 17 products in the FDA NDC directory, labeler code 68546

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

Teva Neuroscience, Inc. (labeler code 68546) lists 17 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 17 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on July 1, 2024.

The request: Watch Teva Neuroscience, Inc. (FDA labeler code 68546): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
68546
Products in commercial distribution
17
Packages
19
Finished drugs by generic name
3
Prescription products
17
Over the counter products
0
Flagged as original packager
4 of 4 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
July 10, 2006
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)17100%

Products by type

TypeProductsShare
Prescription drugs17100%

Drugs it lists

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

DrugProductsCompanies listing it
Deutetrabenazine131
Glatiramer acetate28
Rasagiline mesylate26

Dosage forms

Dosage formProductsShare
Tablet, film coated, extended release847.1%
Tablet, coated317.6%
Injection, solution211.8%
Kit211.8%
Tablet211.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Austedo xr68546-479Tablet, film coated, extended releaseNew drug applications (NDA)July 1, 2024
Austedo xr68546-477KitNew drug applications (NDA)July 1, 2024
Austedo xr68546-476Tablet, film coated, extended releaseNew drug applications (NDA)May 29, 2024
Austedo xr68546-475Tablet, film coated, extended releaseNew drug applications (NDA)May 29, 2024
Austedo xr68546-474Tablet, film coated, extended releaseNew drug applications (NDA)May 29, 2024
Austedo xr68546-473Tablet, film coated, extended releaseNew drug applications (NDA)May 29, 2024
Austedo xr68546-472Tablet, film coated, extended releaseNew drug applications (NDA)February 21, 2023
Austedo xr68546-471Tablet, film coated, extended releaseNew drug applications (NDA)February 21, 2023
Austedo xr68546-470Tablet, film coated, extended releaseNew drug applications (NDA)February 21, 2023
Austedo68546-176KitNew drug applications (NDA)February 1, 2020
Austedo68546-172Tablet, coatedNew drug applications (NDA)April 12, 2017
Austedo68546-171Tablet, coatedNew drug applications (NDA)April 12, 2017
Austedo68546-170Tablet, coatedNew drug applications (NDA)April 12, 2017
Copaxone68546-325Injection, solutionNew drug applications (NDA)January 29, 2014
Copaxone68546-317Injection, solutionNew drug applications (NDA)April 28, 2008
Azilect68546-229TabletNew drug applications (NDA)July 10, 2006
Azilect68546-142TabletNew drug applications (NDA)July 10, 2006

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.