National Drug Code (NDC) Database

Aesica Queenborough Limited

+5

  • NDC:

    43798-014

  • Nonproprietary Name:

    Lumacaftor/Ivacaftor Paediatric

  • Dosage Form:

    TABLET, FILM COATED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    125; 100 mg/1; mg/1

  • Substance:

    IVACAFTOR; LUMACAFTOR

  • Start Marketing Date:

    2017-11-29

  • End Marketing Date:

    2026-10-31

  • DEA Schedule:

  • Certified Through:

    0000-00-00

AGC Biologics A/S

  • NDC:

    82507-004

  • Nonproprietary Name:

    Ustekinumab

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    90 g/L

  • Substance:

    USTEKINUMAB

  • Start Marketing Date:

    2024-07-04

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

AGC Biologics, Inc.

  • NDC:

    83277-005

  • Nonproprietary Name:

    AXATILIMAB

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    50 mg/mL

  • Substance:

    AXATILIMAB

  • Start Marketing Date:

    2024-08-14

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

AGC Inc.

  • NDC:

    75872-0001

  • Nonproprietary Name:

    Tafluprost

  • Dosage Form:

    SOLUTION

  • Product Type:

    BULK INGREDIENT

  • Strength:

    2 g/2g

  • Substance:

    TAFLUPROST

  • Start Marketing Date:

    2011-06-15

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

AGC Pharma Chemicals Europe, S.L.U.

  • NDC:

    65404-010

  • Nonproprietary Name:

    Taletrectinib adipate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TALETRECTINIB ADIPATE

  • Start Marketing Date:

    2026-06-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

AGC WAKASA CHEMICALS CO., LTD.

  • NDC:

    70390-0001

  • Nonproprietary Name:

    Tafluprost

  • Dosage Form:

    SOLUTION

  • Product Type:

    BULK INGREDIENT

  • Strength:

    2 g/2g

  • Substance:

    TAFLUPROST

  • Start Marketing Date:

    2019-10-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

AGC, Inc.

  • NDC:

    75872-0002

  • Nonproprietary Name:

    Perfluorhexlyoctane

  • Dosage Form:

    LIQUID

  • Product Type:

    BULK INGREDIENT

  • Strength:

    200 kg/200kg

  • Substance:

    PERFLUOROHEXYLOCTANE

  • Start Marketing Date:

    2023-01-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Agilent Technologies Inc.

  • NDC:

    70596-1007

  • Nonproprietary Name:

    Plozasiran

  • Dosage Form:

    INJECTION

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    PLOZASIRAN SODIUM

  • Start Marketing Date:

    2025-11-18

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Agilent Technologies, Inc.

  • NDC:

    70596-1004

  • Nonproprietary Name:

    vutrisiran sodium

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    VUTRISIRAN

  • Start Marketing Date:

    2022-06-14

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Aggarwwal Exports

  • NDC:

    72568-000

  • Nonproprietary Name:

    MENTHOL

  • Dosage Form:

    CRYSTAL

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    MENTHOL

  • Start Marketing Date:

    2018-11-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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