National Drug Code (NDC) Database

PolyCarbon Industries, Inc.

  • NDC:

    65571-0022

  • Nonproprietary Name:

    Podophyllotoxin 184

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    PODOFILOX

  • Start Marketing Date:

    2005-10-05

  • End Marketing Date:

    2026-12-21

  • DEA Schedule:

  • Certified Through:

    0000-00-00

PolyPeptide Laboratories (Sweden) AB

  • NDC:

    63586-3602

  • Nonproprietary Name:

    NA1 Hydrochloride

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    2500 g/2500g

  • Substance:

    NERINETIDE HYDROCHLORIDE

  • Start Marketing Date:

    2020-06-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Polypeptide Laboratories San Diego, LLC

  • NDC:

    58862-0179

  • Nonproprietary Name:

    TERLIPRESSIN

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    TERLIPRESSIN

  • Start Marketing Date:

    2022-09-14

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

PolyPeptide Laboratories, Pvt. Ltd.

  • NDC:

    59149-007

  • Nonproprietary Name:

    Octreotide Acetate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    6 g/6g

  • Substance:

    OCTREOTIDE ACETATE

  • Start Marketing Date:

    2023-02-20

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

PPL Pharma Solutions Riverview LLC

  • NDC:

    48957-0121

  • Nonproprietary Name:

    Cabozantinib (S)-malate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    CABOZANTINIB S-MALATE

  • Start Marketing Date:

    2021-02-26

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

PRAVEEN LABORATORIES PRIVATE LIMITED

  • NDC:

    87307-002

  • Nonproprietary Name:

    Clopidogrel Bisulfate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    CLOPIDOGREL BISULFATE

  • Start Marketing Date:

    2026-05-20

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Precision Dose, Inc.

  • NDC:

    68094-075

  • Nonproprietary Name:

    Acetaminophen

  • Dosage Form:

    SUSPENSION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    160 mg/5mL

  • Substance:

    ACETAMINOPHEN

  • Start Marketing Date:

    2024-04-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Premier Dental products

  • NDC:

    10733-802

  • Nonproprietary Name:

    Benzocaine

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    200 mg/mL

  • Substance:

    BENZOCAINE

  • Start Marketing Date:

    2024-12-08

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

PolyPeptide Group

+17

  • NDC:

    68067-2602

  • Nonproprietary Name:

    SEMAGLUTIDE

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    SEMAGLUTIDE

  • Start Marketing Date:

    2020-06-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Porton Pharma Solutions

+9

  • NDC:

    75877-0010

  • Nonproprietary Name:

    Ribociclib Succinate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    RIBOCICLIB SUCCINATE

  • Start Marketing Date:

    2026-05-13

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

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