National Drug Code (NDC) Database

Ipca Laboratories Limited

  • NDC:

    57451-1233

  • Nonproprietary Name:

    Pyrantel Pamoate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    PYRANTEL PAMOATE

  • Start Marketing Date:

    2022-07-22

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Ishihara Sangyo Kaisha, Ltd.

  • NDC:

    64642-011

  • Nonproprietary Name:

    cevimeline

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    20 kg/20kg

  • Substance:

    CEVIMELINE

  • Start Marketing Date:

    2000-03-31

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

ISOMEDIX

  • NDC:

    55718-150

  • Nonproprietary Name:

    Collagenase

  • Dosage Form:

    POWDER

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    1 g/g

  • Substance:

    COLLAGENASE CLOSTRIDIUM HISTOLYTICUM

  • Start Marketing Date:

    2006-10-18

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Isomedix Operations

  • NDC:

    55718-117

  • Nonproprietary Name:

    granisetron

  • Dosage Form:

    INJECTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    10 mg/.4mL

  • Substance:

    GRANISETRON

  • Start Marketing Date:

    2016-08-09

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Isomedix Operations Inc

  • NDC:

    55718-178

  • Nonproprietary Name:

    Eyewash

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    465 mL/473mL

  • Substance:

    WATER

  • Start Marketing Date:

    2025-09-29

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Isomedix Operations Inc.

  • NDC:

    55718-122

  • Nonproprietary Name:

    Water

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    929 g/946mL

  • Substance:

    WATER

  • Start Marketing Date:

    2013-05-24

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Isomedix Operations, Inc

  • NDC:

    55718-164

  • Nonproprietary Name:

    Hydrocotisone Acetate

  • Dosage Form:

    POWDER

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    1 kg/kg

  • Substance:

    HYDROCORTISONE ACETATE

  • Start Marketing Date:

    2023-02-02

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Isomedix Operations, Inc.

  • NDC:

    55718-123

  • Nonproprietary Name:

    Eyewash

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    473 mL/473mL

  • Substance:

    WATER

  • Start Marketing Date:

    2015-01-30

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

ISP Chemicals LLC

  • NDC:

    21222-003

  • Nonproprietary Name:

    FLUNIXIN MEGLUMINE

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    FLUNIXIN MEGLUMINE

  • Start Marketing Date:

    2012-08-06

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Isotopia Molecular Imaging

  • NDC:

    82008-001

  • Nonproprietary Name:

    Lutetium chloride (Lu 177)

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    3000 GBq/mg

  • Substance:

    LUTETIUM LU-177

  • Start Marketing Date:

    2020-08-14

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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