National Drug Code (NDC) Database

Towa Pharmaceutical Europe, S.L.

  • NDC:

    73476-750

  • Nonproprietary Name:

    DULOXETINE HYDROCHLORIDE

  • Dosage Form:

    CAPSULE, DELAYED RELEASE PELLETS

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    40 mg/1

  • Substance:

    DULOXETINE HYDROCHLORIDE

  • Start Marketing Date:

    2018-06-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

TOYOBO CO., LTD.

  • NDC:

    72639-0011

  • Nonproprietary Name:

    mogamulizumab

  • Dosage Form:

    INJECTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    4 mg/mL

  • Substance:

    MOGAMULIZUMAB

  • Start Marketing Date:

    2018-08-08

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Trifarma S.p.A.

  • NDC:

    46204-0371

  • Nonproprietary Name:

    Testosterone Cypionate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TESTOSTERONE CYPIONATE

  • Start Marketing Date:

    2019-09-02

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

    CIII

  • Certified Through:

    2026-12-31

Trifluoperazine Hydrochloride

  • NDC:

    46204-0081

  • Nonproprietary Name:

    Trifluoperazine Hydrochloride

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TRIFLUOPERAZINE HYDROCHLORIDE

  • Start Marketing Date:

    2012-08-16

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Trillium Health Care Products Inc.

  • NDC:

    53592-221

  • Nonproprietary Name:

    Phenylephrine Hydrochloride

  • Dosage Form:

    POWDER

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    22.2 g/kg

  • Substance:

    PHENYLEPHRINE HYDROCHLORIDE

  • Start Marketing Date:

    2022-01-31

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

TRUECARE BIOMEDIX

  • NDC:

    55132-038

  • Nonproprietary Name:

    Aspirin

  • Dosage Form:

    TABLET, COATED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    81 mg/1

  • Substance:

    ASPIRIN

  • Start Marketing Date:

    2024-05-08

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

TYCHE INDUSTRIES LIMITED

  • NDC:

    60862-008

  • Nonproprietary Name:

    TOLVAPTAN

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    100 kg/100kg

  • Substance:

    TOLVAPTAN

  • Start Marketing Date:

    2019-08-26

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

UBE Corporation

  • NDC:

    42672-0100

  • Nonproprietary Name:

    Bepotastine

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    BEPOTASTINE BESILATE

  • Start Marketing Date:

    2009-08-20

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Torrent Pharmaceuticals Limited

  • NDC:

    13668-734

  • Nonproprietary Name:

    Lamotrigine

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    LAMOTRIGINE

  • Start Marketing Date:

    2024-10-04

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Trifarma

+6

  • NDC:

    46204-0121

  • Nonproprietary Name:

    Prochlorperazine Edisylate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    PROCHLORPERAZINE EDISYLATE

  • Start Marketing Date:

    2012-08-02

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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