National Drug Code (NDC) Database

CARBOGEN AMCIS B.V.

  • NDC:

    45408-002

  • Nonproprietary Name:

    CALCIFEDIOL

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    CALCIFEDIOL ANHYDROUS

  • Start Marketing Date:

    2012-08-31

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Cardinal Health 414, LLC

  • NDC:

    65857-800

  • Nonproprietary Name:

    Gallium Chloride GA-68

  • Dosage Form:

    SOLUTION

  • Product Type:

    BULK INGREDIENT

  • Strength:

    400 mCi/mL

  • Substance:

    GALLIUM CHLORIDE GA-68

  • Start Marketing Date:

    2024-04-18

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

CATALENT ARGENTINA S.A.I.C.

  • NDC:

    49588-0005

  • Nonproprietary Name:

    Ibuprofen

  • Dosage Form:

    CAPSULE

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    200 mg/1

  • Substance:

    IBUPROFEN

  • Start Marketing Date:

    2025-06-27

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Catalent Argentina S.A.I.y.C

  • NDC:

    49588-0001

  • Nonproprietary Name:

    Ibuprofen

  • Dosage Form:

    CAPSULE, LIQUID FILLED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    200 mg/1

  • Substance:

    IBUPROFEN

  • Start Marketing Date:

    1995-04-10

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Catalent Germany Schorndorf GmbH

  • NDC:

    68621-0062

  • Nonproprietary Name:

    dutasteride and tamsulosin hydrochloride

  • Dosage Form:

    CAPSULE

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    .5; .4 mg/1; mg/1

  • Substance:

    DUTASTERIDE; TAMSULOSIN HYDROCHLORIDE

  • Start Marketing Date:

    2024-06-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Catalent Indiana, LLC

  • NDC:

    61434-077

  • Nonproprietary Name:

    Aflibercept

  • Dosage Form:

    INJECTION, SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    114.3 mg/mL

  • Substance:

    AFLIBERCEPT

  • Start Marketing Date:

    2025-01-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Catalent Micron Technologies Limited

  • NDC:

    69989-0006

  • Nonproprietary Name:

    Apixaban

  • Dosage Form:

    POWDER

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    1 kg/1

  • Substance:

    APIXABAN

  • Start Marketing Date:

    2016-05-11

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Catalent Micron Technologies Ltd

  • NDC:

    69989-0013

  • Nonproprietary Name:

    Rimegepant

  • Dosage Form:

    POWDER

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    1 kg/1

  • Substance:

    RIMEGEPANT

  • Start Marketing Date:

    2020-10-06

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Catalent Micron Technologies, Inc.

  • NDC:

    69988-0065

  • Nonproprietary Name:

    Gentamicin Sulfate

  • Dosage Form:

    POWDER

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    1 kg/1

  • Substance:

    GENTAMICIN SULFATE

  • Start Marketing Date:

    2025-02-28

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Cargill SLU

  • NDC:

    69507-001

  • Nonproprietary Name:

    DEXTROSE MONOHYDRATE

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    DEXTROSE MONOHYDRATE

  • Start Marketing Date:

    2015-01-09

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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