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Directory/Dr. Reddy's Laboratories Inc.

Dr. Reddy's Laboratories Inc.

Drug manufacturer · manufacturer

Unclaimed listing
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143
Drug products
10
Therapeutic areas

About

Dr. Reddy's Laboratories Inc. is listed in the FDA National Drug Code Directory with 143 marketed products, of which 78 are prescription drugs. Dosage forms include TABLET, INJECTION, CAPSULE, PATCH, LOZENGE. Portfolio includes DEA-scheduled controlled substances.

What Dr. Reddy's Laboratories Inc. makes

16 of 143 products
Clear
Prescription · 78OTC · 65
Other · 78Injectable & Infusion · 28Immunology & Inflammation · 11CNS & Psychiatry · 7Ophthalmic · 7Cardiovascular · 4Gastrointestinal · 4Pain & Anesthesia · 2Anti-infective · 1Dermatology · 1
tablet · 48capsule · 27injection · 26lozenge · 12patch · 6gum · 6kit · 5solution/ drops · 4solution · 4gel · 2
  • Dimethyl Fumarate
    dimethyl fumarate
    Quotecapsule, delayed releaseoralANDA
  • Dimethyl Fumarate
    dimethyl fumarate
    Quotecapsule, delayed releaseoralANDA
  • Lenalidomide
    lenalidomide
    QuotecapsuleoralANDA
  • Lenalidomide
    lenalidomide
    QuotecapsuleoralANDA
  • Lenalidomide
    lenalidomide
    QuotecapsuleoralANDA
  • Lenalidomide
    lenalidomide
    QuotecapsuleoralANDA
  • Lenalidomide
    lenalidomide
    QuotecapsuleoralANDA
  • Lenalidomide
    lenalidomide
    QuotecapsuleoralANDA
  • Lubiprostone
    lubiprostone
    Quotecapsule, gelatin coatedoralNDA AUTHORIZED GENERIC
  • Lubiprostone
    lubiprostone
    Quotecapsule, gelatin coatedoralNDA AUTHORIZED GENERIC
  • METYROSINE
    metyrosine
    QuotecapsuleoralANDA
  • Nintedanib
    nintedanib
    QuotecapsuleoralANDA
  • Nintedanib
    nintedanib
    QuotecapsuleoralANDA
  • Sertraline Hydrochloride
    sertraline hydrochloride
    QuotecapsuleoralANDA
  • Sertraline Hydrochloride
    sertraline hydrochloride
    QuotecapsuleoralANDA
  • Gas Relief
    simethicone capsules usp, 125 mg
    Quotecapsule, liquid filledoralOTC MONOGRAPH DRUG

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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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