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Directory/ScieGen Pharmaceuticals, Inc

ScieGen Pharmaceuticals, Inc

Drug manufacturer · manufacturer

Unclaimed listing
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38
Drug products
5
Therapeutic areas

About

ScieGen Pharmaceuticals, Inc is listed in the FDA National Drug Code Directory with 38 marketed products, of which 38 are prescription drugs. Dosage forms include TABLET, CAPSULE, SOLUTION. Portfolio includes DEA-scheduled controlled substances.

What ScieGen Pharmaceuticals, Inc makes

22 of 38 products
Clear
Prescription · 38
Other · 22Cardiovascular · 8CNS & Psychiatry · 5Immunology & Inflammation · 2Anti-infective · 1
tablet · 21capsule · 16solution · 1
  • Fluoxetine
    fluoxetine
    Quotetablet, film coatedoralANDA
  • Fluoxetine
    fluoxetine
    Quotetablet, film coatedoralANDA
  • Levetiracetam
    levetiracetam
    Quotetablet, film coated, extended releaseoralANDA
  • Levetiracetam
    levetiracetam
    Quotetablet, film coated, extended releaseoralANDA
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • Pregabalin
    pregabalin
    QuotecapsuleoralANDACV
  • RANOLAZINE
    ranolazine
    Quotetablet, film coated, extended releaseoralANDA
  • RANOLAZINE
    ranolazine
    Quotetablet, film coated, extended releaseoralANDA

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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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