National Drug Code (NDC) Database

Bayer AG

+39

  • NDC:

    12866-3230

  • Nonproprietary Name:

    Gadoquatrane

  • Dosage Form:

    INJECTION

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    257.9 mg/mL

  • Substance:

    GADOQUATRANE

  • Start Marketing Date:

    2026-06-12

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Bausch Health Companies Inc.

  • NDC:

    62660-150

  • Nonproprietary Name:

    Rifaximin

  • Dosage Form:

    TABLET, COATED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    550 mg/1

  • Substance:

    RIFAXIMIN

  • Start Marketing Date:

    2010-05-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Bausch Health Ireland Limited

  • NDC:

    71071-001

  • Nonproprietary Name:

    fluocinolone acetonide implant

  • Dosage Form:

    IMPLANT

  • Product Type:

    BULK INGREDIENT

  • Strength:

    0.59 mg/.59mg

  • Substance:

    FLUOCINOLONE ACETONIDE

  • Start Marketing Date:

    2008-08-08

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Bayer de Mexico, S.A. de C.V.

  • NDC:

    12875-9951

  • Nonproprietary Name:

    Testosterone Enanthate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TESTOSTERONE ENANTHATE

  • Start Marketing Date:

    2014-04-28

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

    CIII

  • Certified Through:

    2027-12-31

Bayer HealthCare LLC

  • NDC:

    0280-1199

  • Nonproprietary Name:

    Dextromethorphan Hydrobromide, Paracetamol, Phenylephrine Hydrochloride

  • Dosage Form:

    CAPSULE, LIQUID FILLED

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    325; 10; 5 mg/1; mg/1; mg/1

  • Substance:

    ACETAMINOPHEN; DEXTROMETHORPHAN HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE

  • Start Marketing Date:

    2017-01-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Bayer HealthCare LLC.

  • NDC:

    11523-8258

  • Nonproprietary Name:

    docusate sodium

  • Dosage Form:

    CAPSULE

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    100 mg/1

  • Substance:

    DOCUSATE SODIUM

  • Start Marketing Date:

    2025-12-15

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Bayer Healthcare Manufacturing Srl

  • NDC:

    23070-8513

  • Nonproprietary Name:

    Ciprofloxacin

  • Dosage Form:

    TABLET

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    500 mg/1

  • Substance:

    CIPROFLOXACIN

  • Start Marketing Date:

    2024-07-09

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Bayer HealthCare Pharmaceuticals Inc.

  • NDC:

    50419-542

  • Nonproprietary Name:

    Finerenone

  • Dosage Form:

    TABLET

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    40 mg/1

  • Substance:

    FINERENONE

  • Start Marketing Date:

    2025-07-13

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Bayer Hispania, S.L.

  • NDC:

    53599-128

  • Nonproprietary Name:

    ASPIRIN

  • Dosage Form:

    CRYSTAL

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    ASPIRIN

  • Start Marketing Date:

    1989-02-08

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

BCN Peptides

+14

  • NDC:

    35207-0015

  • Nonproprietary Name:

    Tetracosactide

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 g/g

  • Substance:

    COSYNTROPIN

  • Start Marketing Date:

    2026-06-15

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

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