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Data / Drug companies / Vivus LLC

Vivus LLC: 10 products in the FDA NDC directory, labeler code 62541

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

Vivus LLC (labeler code 62541) lists 10 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 10 prescription drugs. Its main marketing category is biologics (BLA). The newest product started marketing on July 1, 2021.

The request: Watch Vivus LLC (FDA labeler code 62541): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
62541
Products in commercial distribution
10
Packages
11
Finished drugs by generic name
1
Prescription products
10
Over the counter products
0
Controlled substance products
Schedule IV 4
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 12, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Biologics (BLA)660%
New drug applications (NDA)440%

Products by type

TypeProductsShare
Prescription drugs10100%

Drugs it lists

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

DrugProductsCompanies listing it
Phentermine and topiramate43

Dosage forms

Dosage formProductsShare
Capsule, delayed release660%
Capsule, extended release440%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Pancreaze62541-406Capsule, delayed releaseBiologics (BLA)July 1, 2021
Pancreaze62541-401Capsule, delayed releaseBiologics (BLA)August 1, 2016
Qsymia62541-204Capsule, extended releaseNew drug applications (NDA)September 17, 2012
Qsymia62541-203Capsule, extended releaseNew drug applications (NDA)September 17, 2012
Qsymia62541-202Capsule, extended releaseNew drug applications (NDA)September 17, 2012
Qsymia62541-201Capsule, extended releaseNew drug applications (NDA)September 17, 2012
Pancreaze62541-405Capsule, delayed releaseBiologics (BLA)April 12, 2010
Pancreaze62541-404Capsule, delayed releaseBiologics (BLA)April 12, 2010
Pancreaze62541-403Capsule, delayed releaseBiologics (BLA)April 12, 2010
Pancreaze62541-402Capsule, delayed releaseBiologics (BLA)April 12, 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.