National Drug Code (NDC) Database

Olon SpA

  • NDC:

    17337-0545

  • Nonproprietary Name:

    Glycopirronium Bromide

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    GLYCOPYRROLATE

  • Start Marketing Date:

    2017-03-03

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Olon USA LLC

  • NDC:

    71604-0002

  • Nonproprietary Name:

    Aceclidine HCl

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    ACECLIDINE HYDROCHLORIDE

  • Start Marketing Date:

    2022-10-24

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Olon, SpA

  • NDC:

    17337-0423

  • Nonproprietary Name:

    Pyridoxine Dipalmitate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    PYRIDOXINE DIPALMITATE

  • Start Marketing Date:

    2017-02-13

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Olpha AS

  • NDC:

    63818-0435

  • Nonproprietary Name:

    AMANTADINE HYDROCHLORIDE

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    AMANTADINE HYDROCHLORIDE

  • Start Marketing Date:

    2016-05-05

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

OMRIX BIOPHARMACEUTICALS LTD

  • NDC:

    67778-100

  • Nonproprietary Name:

    Human Thrombin

  • Dosage Form:

    SOLUTION

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    HUMAN THROMBIN

  • Start Marketing Date:

    2009-09-19

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Omya Inc.

  • NDC:

    67054-005

  • Nonproprietary Name:

    Calcium Carbonate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    CALCIUM CARBONATE

  • Start Marketing Date:

    2009-09-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Ono Pharmaceutical Co., Ltd.

  • NDC:

    63902-100

  • Nonproprietary Name:

    Alprostadil

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    ALPROSTADIL

  • Start Marketing Date:

    2012-01-15

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

OPELLA HEALTHCARE INTERNATIONAL SAS

  • NDC:

    12579-510

  • Nonproprietary Name:

    leflunomide

  • Dosage Form:

    TABLET, FILM COATED

  • Product Type:

    BULK INGREDIENT

  • Strength:

    20 mg/1

  • Substance:

    LEFLUNOMIDE

  • Start Marketing Date:

    1998-09-10

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Opocrin SpA

+1

  • NDC:

    46575-002

  • Nonproprietary Name:

    Iron Sucrose

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    IRON SUCROSE

  • Start Marketing Date:

    2025-08-08

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Olymel

  • NDC:

    59238-100

  • Nonproprietary Name:

    crude heparin

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    HEPARIN SODIUM

  • Start Marketing Date:

    2006-12-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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