National Drug Code (NDC) Database

Evonik Operations GmbH

  • NDC:

    52696-0010

  • Nonproprietary Name:

    Vonoprazan Fumarate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    VONOPRAZAN FUMARATE

  • Start Marketing Date:

    2023-11-21

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Evonik Rexim (Nanning) Pharmaceutical Co. Ltd.

  • NDC:

    16947-8203

  • Nonproprietary Name:

    L-Aspartic Acid

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    ASPARTIC ACID

  • Start Marketing Date:

    2006-08-28

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Evonik Rexim (Nanning) Pharmaceutical Co., Ltd.

  • NDC:

    16947-8207

  • Nonproprietary Name:

    L-Serine

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    SERINE

  • Start Marketing Date:

    2023-08-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Evonik Rexim S.A.S.

  • NDC:

    51593-5005

  • Nonproprietary Name:

    L-Alanyl-L-Glutamine

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    ALANYL GLUTAMINE

  • Start Marketing Date:

    1992-01-03

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Excella GmbH & Co KG

  • NDC:

    46014-6202

  • Nonproprietary Name:

    busulfan

  • Dosage Form:

    TABLET, FILM COATED

  • Product Type:

    HUMAN PRESCRIPTION DRUG

  • Strength:

    2 mg/1

  • Substance:

    BUSULFAN

  • Start Marketing Date:

    2023-05-15

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Excella GmbH & Co. KG

  • NDC:

    46014-9076

  • Nonproprietary Name:

    paroxetine

  • Dosage Form:

    CAPSULE

  • Product Type:

    HUMAN PRESCRIPTION DRUG

  • Strength:

    7.5 mg/1

  • Substance:

    PAROXETINE MESYLATE

  • Start Marketing Date:

    2025-02-18

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Excella GmbH & Co.KG

  • NDC:

    46014-1098

  • Nonproprietary Name:

    Adapalene

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    ADAPALENE

  • Start Marketing Date:

    2011-05-25

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Excella GmbH & Cp. KG

  • NDC:

    46014-1004

  • Nonproprietary Name:

    Ganciclovir anhydrous

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    2-AMINO-9-(((1RS)-2-CHLORO-1-(HYDROXYMETHYL)ETHOXY)METHYL)-1,9-DIHYDRO-6H-PURIN-6-ONE

  • Start Marketing Date:

    2001-08-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Excella GmbH &Co.KG

  • NDC:

    46014-1019

  • Nonproprietary Name:

    Acyclovir Sodium

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    ACYCLOVIR SODIUM

  • Start Marketing Date:

    2016-12-16

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Evonik

+17

  • NDC:

    72309-004

  • Nonproprietary Name:

    Olanzapine Pamoate

  • Dosage Form:

    POWDER, FOR SUSPENSION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    1 mg/mg

  • Substance:

    OLANZAPINE PAMOATE

  • Start Marketing Date:

    2025-01-22

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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