National Drug Code (NDC) Database

Deretil SA

  • NDC:

    67367-555

  • Nonproprietary Name:

    Amoxicillin Trihydrate

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    25 kg/25kg

  • Substance:

    AMOXICILLIN

  • Start Marketing Date:

    2009-05-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Derivados Quimicos

  • NDC:

    59349-0038

  • Nonproprietary Name:

    Terbinafine Hydrochloride

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    TERBINAFINE HYDROCHLORIDE

  • Start Marketing Date:

    2023-03-03

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Dermaceutical Laboratories Limited Liability Company

  • NDC:

    22647-028

  • Nonproprietary Name:

    ZINC OXIDE

  • Dosage Form:

    STICK

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    10 g/100g

  • Substance:

    ZINC OXIDE

  • Start Marketing Date:

    2021-05-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

DERMSTORY CO, LTD

  • NDC:

    80625-0005

  • Nonproprietary Name:

    Zinc Oxide

  • Dosage Form:

    PASTE

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    48 kg/100kg

  • Substance:

    ZINC OXIDE

  • Start Marketing Date:

    2025-06-01

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Deseret Biolgicals, Inc.

  • NDC:

    43742-2275

  • Nonproprietary Name:

    Helicobacter Pylori, Helicobacter Pylori DNA

  • Dosage Form:

    LIQUID

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    10; 10 mL; mL

  • Substance:

    HELICOBACTER PYLORI; HELICOBACTER PYLORI DNA

  • Start Marketing Date:

    2025-04-29

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Deseret Biologicals

  • NDC:

    43742-2273

  • Nonproprietary Name:

    Enterococcus Faecalis, Pneumococcinum, Streptococcus Agalactiae, Streptococcus Agalactiae DNA, Streptococcus Bovis, Streptococcus Dysgalactiae, Streptococcus Dysgalactiae DNA, Streptococcus Mutans, Streptococcus Mutans DNA, Streptococcus Oralis, Streptoco

  • Dosage Form:

    LIQUID

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    500; 500; 500; 500; 500; 500; 500; 500; 500; 500 mL; mL; mL; mL; mL; mL; mL; mL; mL; mL

  • Substance:

    ENTEROCOCCUS FAECALIS; HERRING SPERM DNA; STREPTOCOCCUS AGALACTIAE; STREPTOCOCCUS DYSGALACTIAE; STREPTOCOCCUS EQUINUS; STREPTOCOCCUS MUTANS; STREPTOCOCCUS ORALIS; STREPTOCOCCUS PNEUMONIAE; STREPTOCOCCUS UBERIS; STREPTOCOCCUS VIRIDANS GROUP

  • Start Marketing Date:

    2025-05-06

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Deseret Biologicals, Inc

  • NDC:

    43742-2189

  • Nonproprietary Name:

    Giardia Lamblia, Giardia Lamblia DNA

  • Dosage Form:

    LIQUID

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    1; 1 mL; mL

  • Substance:

    GIARDIA LAMBLIA; GIARDIA LAMBLIA DNA

  • Start Marketing Date:

    2024-08-19

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

Deseret Biologicals, Inc.

  • NDC:

    43742-2535

  • Nonproprietary Name:

    Herpes Simplex Nosode I and II DNA

  • Dosage Form:

    LIQUID

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    10 mL

  • Substance:

    HERRING SPERM DNA

  • Start Marketing Date:

    2026-02-20

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Delta Synthetic Co. Ltd

+3

  • NDC:

    60203-1004

  • Nonproprietary Name:

    Guaifenesin DC95

  • Dosage Form:

    GRANULE

  • Product Type:

    DRUG FOR FURTHER PROCESSING

  • Strength:

    950 g/kg

  • Substance:

    GUAIFENESIN

  • Start Marketing Date:

    2021-01-25

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2027-12-31

Derivados Quimicos SAU

+12

  • NDC:

    59349-0042

  • Nonproprietary Name:

    Domperidone

  • Dosage Form:

    POWDER

  • Product Type:

    BULK INGREDIENT

  • Strength:

    1 kg/kg

  • Substance:

    DOMPERIDONE

  • Start Marketing Date:

    2025-10-23

  • End Marketing Date:

    0000-00-00

  • DEA Schedule:

  • Certified Through:

    2026-12-31

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