National Drug Code (NDC) Database

Pfizer Laboratories Div Pfizer Inc

  • NDC:

    0069-4270

  • Nonproprietary Name:

    prazosin hydrochloride

  • Dosage Form:

    TABLET

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    5 mg/1

  • Substance:

    PRAZOSIN HYDROCHLORIDE

  • Start Marketing Date:

    2014-09-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Pfizer Manufacturing Belgium NV

  • NDC:

    59267-9401

  • Nonproprietary Name:

    pegvisomant

  • Dosage Form:

    INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    20 mg/mL

  • Substance:

    PEGVISOMANT

  • Start Marketing Date:

    2013-03-11

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Pfizer Manufacturing Deutschland GmbH

  • NDC:

    53869-4960

  • Nonproprietary Name:

    sertraline hydrochloride

  • Dosage Form:

    TABLET, FILM COATED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    25 mg/1

  • Substance:

    SERTRALINE HYDROCHLORIDE

  • Start Marketing Date:

    2020-10-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Pfizer Manufacturing Deutschland GmbH (Betriebsstätte Freiburg)

  • NDC:

    53869-2231

  • Nonproprietary Name:

    CRIZOTINIB

  • Dosage Form:

    CAPSULE

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    200 mg/1

  • Substance:

    CRIZOTINIB

  • Start Marketing Date:

    2011-09-30

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Pharma Source Direct, Inc.

  • NDC:

    82393-601

  • Nonproprietary Name:

    Testosterone Enanthate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TESTOSTERONE ENANTHATE

  • Start Marketing Date:

    2026-03-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

    CIII

  • Certified Through:

    2027-12-31

Pharmaceutical Works POLPHARMA

  • NDC:

    12658-0635

  • Nonproprietary Name:

    ARIPIPRAZOLE LAUROXIL

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    20 kg/20kg

  • Substance:

    ARIPIPRAZOLE LAUROXIL

  • Start Marketing Date:

    2015-10-05

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Pharmacia & Upjohn Company LLC

  • NDC:

    0995-8721

  • Nonproprietary Name:

    Oclacitinib Maleate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    OCLACITINIB MALEATE

  • Start Marketing Date:

    2011-10-06

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Pharmacia and Upjohn Company LLC

  • NDC:

    0009-5620

  • Nonproprietary Name:

    Progesterone

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    PROGESTERONE

  • Start Marketing Date:

    2014-07-03

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Pfizer Inc

+9

  • NDC:

    65427-416

  • Nonproprietary Name:

    azithromycin dihydrate

  • Dosage Form:

    TABLET, FILM COATED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    500 mg/1

  • Substance:

    AZITHROMYCIN DIHYDRATE

  • Start Marketing Date:

    2022-07-11

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Actylis

+1

  • NDC:

    12562-3023

  • Nonproprietary Name:

    Adenosine

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    ADENOSINE

  • Start Marketing Date:

    2023-12-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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