National Drug Code (NDC) Database

Gehring-Montgomery, Inc

  • NDC:

    63163-002

  • Nonproprietary Name:

    PROPYLENE GLYCOL

  • Dosage Form:

    LIQUID

  • Product Type:

    BULK INGREDIENT

  • Strength:

    100 kg/100kg

  • Substance:

    PROPYLENE GLYCOL

  • Start Marketing Date:

    1984-01-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Gemini PharmChem Mannheim GmbH

  • NDC:

    77391-005

  • Nonproprietary Name:

    Valrubicin

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    VALRUBICIN

  • Start Marketing Date:

    2021-08-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Genentech, Inc.

  • NDC:

    50242-931

  • Nonproprietary Name:

    somatropin

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    5 g/2L

  • Substance:

    SOMATROPIN

  • Start Marketing Date:

    1995-12-29

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Genentech, Inc. (SSF)

  • NDC:

    50242-160

  • Nonproprietary Name:

    Bevacizumab

  • Dosage Form:

    LIQUID

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    25 g/L

  • Substance:

    BEVACIZUMAB

  • Start Marketing Date:

    2004-02-26

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

GenIbet Biopharmaceuticals

  • NDC:

    83461-400

  • Nonproprietary Name:

    Fecal Microbiota Spores, Live-brpk

  • Dosage Form:

    CAPSULE

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    30000000 [CFU]/1

  • Substance:

    DONOR HUMAN STOOL SPORES (ETHANOL TREATED)

  • Start Marketing Date:

    2023-04-26

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

GENTEC S.A.

  • NDC:

    81997-001

  • Nonproprietary Name:

    Latanoprost

  • Dosage Form:

    OIL

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    LATANOPROST

  • Start Marketing Date:

    2021-07-12

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

GenTrac Inc.

  • NDC:

    52766-0100

  • Nonproprietary Name:

    thrombin

  • Dosage Form:

    LIQUID

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    THROMBIN

  • Start Marketing Date:

    1986-02-03

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Genzyme Corporation

  • NDC:

    58468-5151

  • Nonproprietary Name:

    Dupilumab

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    175 mg/mL

  • Substance:

    DUPILUMAB

  • Start Marketing Date:

    2020-08-18

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Genzyme Ireland Limited

  • NDC:

    83246-065

  • Nonproprietary Name:

    efanesoctocog alfa

  • Dosage Form:

    POWDER, FOR SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    4000 [iU]/3mL

  • Substance:

    EFANESOCTOCOG ALFA

  • Start Marketing Date:

    2024-08-07

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Genvion Corporation

+2

  • NDC:

    62049-185

  • Nonproprietary Name:

    FLUOROURACIL

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    FLUOROURACIL

  • Start Marketing Date:

    2019-05-07

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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