National Drug Code (NDC) Database

Ames Goldsmith Corp.

  • NDC:

    50828-001

  • Nonproprietary Name:

    SILVER NITRATE

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    SILVER NITRATE

  • Start Marketing Date:

    2011-12-07

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Amgen, Inc

  • NDC:

    55513-834

  • Nonproprietary Name:

    Brodalumab

  • Dosage Form:

    SOLUTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    140 mg/mL

  • Substance:

    BRODALUMAB

  • Start Marketing Date:

    2017-02-15

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Amicogen(China) Biopharm Co., Ltd

  • NDC:

    71411-0004

  • Nonproprietary Name:

    Tulathromycin

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TULATHROMYCIN

  • Start Marketing Date:

    2017-06-07

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Amigo & Arditi S.A.

  • NDC:

    87074-000

  • Nonproprietary Name:

    MENTHOL

  • Dosage Form:

    CRYSTAL

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    MENTHOL

  • Start Marketing Date:

    1977-01-03

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Amino Chemicals Ltd

  • NDC:

    66005-0050

  • Nonproprietary Name:

    Paliperidone

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    PALIPERIDONE

  • Start Marketing Date:

    2022-06-07

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Amivas, Inc

  • NDC:

    73607-003

  • Nonproprietary Name:

    Phosphate Buffer

  • Dosage Form:

    SOLUTION

  • Product Type:

    HUMAN PRESCRIPTION DRUG

  • Strength:

    443.6; 24.1 mg/1; mg/1

  • Substance:

    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

  • Start Marketing Date:

    2020-12-11

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Shandong Awa Biopharma

  • NDC:

    83428-001

  • Nonproprietary Name:

    Sodium Hyaluronate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    HYALURONATE SODIUM

  • Start Marketing Date:

    2023-04-26

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Ami Lifesciences Private Limited

+4

  • NDC:

    59680-018

  • Nonproprietary Name:

    Tadalafil

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TADALAFIL

  • Start Marketing Date:

    2024-11-30

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Amino Chemicals

  • NDC:

    66005-0029

  • Nonproprietary Name:

    Rasagiline Mesylate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    RASAGILINE MESYLATE

  • Start Marketing Date:

    2009-05-14

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

AMINO GmbH

  • NDC:

    46052-0196

  • Nonproprietary Name:

    Betaine anhydrous

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    BETAINE

  • Start Marketing Date:

    1997-01-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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