National Drug Code (NDC) Database

Bio-Technology General (Israel) Ltd.

  • NDC:

    84606-6824

  • Nonproprietary Name:

    Pegloticase

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    8 mg/mL

  • Substance:

    PEGLOTICASE

  • Start Marketing Date:

    2010-12-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

BIOBEAUTECH Co., Ltd.

  • NDC:

    83697-010

  • Nonproprietary Name:

    Zinc Oxide

  • Dosage Form:

    POWDER

  • Product Type:

    HUMAN OTC DRUG

  • Strength:

    99.99 kg/100kg

  • Substance:

    ZINC OXIDE

  • Start Marketing Date:

    2023-08-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

BIOBLOOM INC.

  • NDC:

    87079-500

  • Nonproprietary Name:

    FOXO4-DRI Synthetic Peptide

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    CAT FEL D 1 SYNTHETIC PEPTIDE (CPAVKRDVDLFLT)

  • Start Marketing Date:

    2025-09-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

BioChem Oss

  • NDC:

    84031-0467

  • Nonproprietary Name:

    Heparin Sodium

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    HEPARIN SODIUM

  • Start Marketing Date:

    2020-03-17

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Biocon Biologics Limited

  • NDC:

    82196-020

  • Nonproprietary Name:

    Insulin

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    28.5 mg/g

  • Substance:

    INSULIN HUMAN

  • Start Marketing Date:

    2024-12-11

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

BioConnection B.V.

  • NDC:

    70383-130

  • Nonproprietary Name:

    USTEKINUMAB

  • Dosage Form:

    INJECTION, SOLUTION, CONCENTRATE

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    5 mg/mL

  • Substance:

    USTEKINUMAB

  • Start Marketing Date:

    2025-03-03

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Biofer SpA

+1

  • NDC:

    44498-002

  • Nonproprietary Name:

    HEPARIN SODIUM

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    HEPARIN SODIUM

  • Start Marketing Date:

    2018-12-18

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Biogen Inc.

  • NDC:

    64406-715

  • Nonproprietary Name:

    EFANESOCTOCOG ALFA

  • Dosage Form:

    POWDER, FOR SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    4000 [iU]/1

  • Substance:

    EFANESOCTOCOG ALFA

  • Start Marketing Date:

    2023-02-22

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Biocon

+61

  • NDC:

    65727-115

  • Nonproprietary Name:

    Trametinib Dimethylsulfoxide

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TRAMETINIB DIMETHYL SULFOXIDE

  • Start Marketing Date:

    2026-03-20

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Biogen

+1

  • NDC:

    64406-311

  • Nonproprietary Name:

    Nusinersen

  • Dosage Form:

    INJECTION, SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    10 mg/mL

  • Substance:

    NUSINERSEN

  • Start Marketing Date:

    2025-05-18

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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