Sun Pharmaceutical Industries, Inc.
Drug manufacturer · manufacturer
Unclaimed listing
721
Drug products
13
Therapeutic areas
About
Sun Pharmaceutical Industries, Inc. is listed in the FDA National Drug Code Directory with 721 marketed products, of which 664 are prescription drugs. Dosage forms include CAPSULE, CREAM, SOLUTION, KIT, INJECTION. Portfolio includes DEA-scheduled controlled substances.
What Sun Pharmaceutical Industries, Inc. makes
721 productsOther · 321Immunology & Inflammation · 103CNS & Psychiatry · 69Anti-infective · 58Cardiovascular · 50Dermatology · 35Injectable & Infusion · 24Pain & Anesthesia · 23Nutrition & Supplements · 22Hormones & Endocrine · 11
tablet · 319capsule · 135cream · 66injection · 41solution · 39ointment · 24gel · 20suspension · 18solution/ drops · 9lotion · 9
- YONSAabiraterone acetatetabletoralNDA
- FeverallacetaminophensuppositoryrectalNDA
- FeverallacetaminophensuppositoryrectalNDA
- FeverallacetaminophensuppositoryrectalNDA
- FeverAllacetaminophensuspensionoralOTC MONOGRAPH DRUG
- Acetaminophen 250 mg and Ibuprofen 125 mgacetaminophen 250 mg and ibuprofen 125 mg tabletstabletoralANDA
- AcycloviracyclovirointmenttopicalANDA
- AcycloviracyclovircreamtopicalANDA
- AdapaleneadapalenegeltopicalANDA
- AdapaleneadapalenegeltopicalANDA
- Adapalene and Benzoyl Peroxideadapalene and benzoyl peroxidegeltopicalANDA
- ADAPALENE and BENZOYL PEROXIDEadapalene and benzoyl peroxidegeltopicalANDA
- albuterol sulfatealbuterol sulfatetabletoralANDA
- albuterol sulfatealbuterol sulfatetabletoralANDA
- Albuterol Sulfatealbuterol sulfatesolutionrespiratory (inhalation)ANDA
- Alclometasone Dipropionatealclometasone dipropionateointmenttopicalANDA
- Alclometasone dipropionatealclometasone dipropionatecreamtopicalANDA
- Alfuzosin Hydrochloridealfuzosin hydrochloridetablet, extended releaseoralANDA
- AllopurinolallopurinoltabletoralANDA
- AllopurinolallopurinoltabletoralANDA
- ambrisentanambrisentantablet, film coatedoralANDA
- ambrisentanambrisentantablet, film coatedoralANDA
- AmcinonideamcinonideointmenttopicalANDA
- Amiodarone Hydrochlorideamiodarone hydrochloridetabletoralANDA
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From the FDA NDC Directory, refreshed 2026-08-15.
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