National Drug Code (NDC) Database

MEDGEL PRIVATE LIMITED

  • NDC:

    51344-928

  • Nonproprietary Name:

    Bismuth subsalicylate

  • Dosage Form:

    CAPSULE, LIQUID FILLED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    262 mg/1

  • Substance:

    BISMUTH SUBSALICYLATE

  • Start Marketing Date:

    2025-03-24

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Medi-Physics Inc. dba GE Healthcare

  • NDC:

    17156-946

  • Nonproprietary Name:

    SODIUM THIOSULFATE

  • Dosage Form:

    SOLUTION

  • Product Type:

    BULK INGREDIENT

  • Strength:

    600 mCi/600mCi

  • Substance:

    SODIUM THIOSULFATE

  • Start Marketing Date:

    2013-07-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Medichem Manufacturing (Malta) Ltd.

  • NDC:

    16436-0132

  • Nonproprietary Name:

    Ivacaftor

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    75 kg/75kg

  • Substance:

    IVACAFTOR

  • Start Marketing Date:

    2024-08-02

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Medichem S.A.

  • NDC:

    53296-0132

  • Nonproprietary Name:

    Ivacaftor

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    75 kg/75kg

  • Substance:

    IVACAFTOR

  • Start Marketing Date:

    2024-08-02

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Medilane Healthcare Pvt Ltd

  • NDC:

    85955-002

  • Nonproprietary Name:

    CYANOCOBALAMIN

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    100 g/100g

  • Substance:

    CYANOCOBALAMIN

  • Start Marketing Date:

    2025-07-22

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Medilux Laboratories Private Limited

  • NDC:

    50218-017

  • Nonproprietary Name:

    Bumetanide

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    BUMETANIDE

  • Start Marketing Date:

    2025-04-25

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Medilux Laboratories Pvt. Ltd.

  • NDC:

    50218-009

  • Nonproprietary Name:

    Hydroquinone

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    HYDROQUINONE

  • Start Marketing Date:

    2012-07-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

MedImmune, U.K. Limited

  • NDC:

    66020-051

  • Nonproprietary Name:

    Influenza Vaccine Live Intranasal

  • Dosage Form:

    SPRAY

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    1000000; 1000000 [FFU]/125mL; [FFU]/125mL

  • Substance:

    INFLUENZA A VIRUS; INFLUENZA B VIRUS

  • Start Marketing Date:

    2007-02-23

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

McNeil AB

  • NDC:

    28663-009

  • Nonproprietary Name:

    Nicotine

  • Dosage Form:

    SPRAY, METERED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    10 mg/mL

  • Substance:

    NICOTINE

  • Start Marketing Date:

    1996-05-22

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Medisca

+3

  • NDC:

    38779-3335

  • Nonproprietary Name:

    Vitamin D3 (Dry)

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    VITAMIN D

  • Start Marketing Date:

    2025-08-05

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

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