Data / Drug companies / Sanofi-Aventis U.S. LLC

Sanofi-Aventis U.S. LLC: 16 products in the FDA NDC directory, labeler code 0075

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

Sanofi-Aventis U.S. LLC (labeler code 0075) lists 16 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 16 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on March 29, 1993.

The request: Watch Sanofi-Aventis U.S. LLC (FDA labeler code 0075): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code

0075

Products in commercial distribution

16

Packages

16

Finished drugs by generic name

1

Prescription products

16

Over the counter products

0

Flagged as original packager

16 of 16 products that carry the flag

Started marketing in the last 12 months

0

Earliest marketing start

March 29, 1993

openFDA record search

api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Products by type

Drugs it lists

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

Dosage forms

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

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.