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Directory/Sanofi-Aventis U.S. LLC

Sanofi-Aventis U.S. LLC

Drug manufacturer · manufacturer

Unclaimed listing
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82
Drug products
7
Therapeutic areas

About

Sanofi-Aventis U.S. LLC is listed in the FDA National Drug Code Directory with 82 marketed products, of which 82 are prescription drugs. Dosage forms include INJECTION, TABLET, KIT, SOLUTION, POWDER. Portfolio includes DEA-scheduled controlled substances.

What Sanofi-Aventis U.S. LLC makes

17 of 82 products
Clear
Prescription · 82
Injectable & Infusion · 41Other · 16Diabetes & Metabolic · 14Biologics & Vaccines · 3Cardiovascular · 3Immunology & Inflammation · 3Anti-infective · 2
injection · 57tablet · 17kit · 4solution · 2powder · 2
  • Plavix
    clopidogrel
    Quotetablet, film coatedoralNDA
  • Plavix
    clopidogrel
    Quotetablet, film coatedoralNDA
  • Multaq
    dronedarone
    Quotetablet, film coatedoralNDA
  • Fexinidazole
    fexinidazole
    QuotetabletoralNDA
  • Avapro
    irbesartan
    Quotetablet, film coatedoralNDA
  • Avapro
    irbesartan
    Quotetablet, film coatedoralNDA
  • Avalide
    irbesartan and hydrochlorothiazide
    Quotetablet, film coatedoralNDA
  • Avalide
    irbesartan and hydrochlorothiazide
    Quotetablet, film coatedoralNDA
  • Arava
    leflunomide
    Quotetablet, film coatedoralNDA
  • Arava
    leflunomide
    Quotetablet, film coatedoralNDA
  • Arava
    leflunomide
    Quotetablet, film coatedoralNDA
  • Primaquine Phosphate
    primaquine phosphate
    Quotetablet, film coatedoralNDA
  • Priftin
    rifapentine
    Quotetablet, film coatedoralNDA
  • Sevelamer Carbonate
    sevelamer carbonate
    Quotetablet, film coatedoralNDA AUTHORIZED GENERIC
  • Sevelamer Carbonate
    sevelamer carbonate
    Quotetablet, film coatedoralNDA AUTHORIZED GENERIC
  • Ambien
    zolpidem tartrate
    Quotetablet, film coatedoralNDACIV
  • Ambien
    zolpidem tartrate
    Quotetablet, film coatedoralNDACIV

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Contact

Email and website are not published in the public registries — they are added when the listing is claimed.

From the FDA NDC Directory, refreshed 2026-08-15.

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