NDC 43742-0754

Coumarin

Coumarinum

Coumarin is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Coumarin.

• Product ID: 43742-0754_1c49962e-663c-463f-8bd2-5b0c05ba794b
• NDC: 43742-0754
• Product Type: Human Otc Drug
• Proprietary Name: Coumarin
• Generic Name: Coumarinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2016-05-06
• Marketing End Date: 2022-11-16
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: COUMARIN
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0754-1

30 mL in 1 BOTTLE, DROPPER (43742-0754-1)

• Marketing Start Date: 2016-05-06
• Marketing End Date: 2022-11-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0754-1 [43742075401]

Coumarin LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-05-06
• Marketing End Date: 2022-11-16

Drug Details

Active Ingredients

Ingredient	Strength
COUMARIN	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 36991316-588b-408e-acf9-a4ca5e8c12e9
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • A4VZ22K1WT

NDC Crossover Matching brand name "Coumarin" or generic name "Coumarinum"

NDC	Brand Name	Generic Name
43742-0754	Coumarin	Coumarinum
43857-0272	Coumarin	Not applicable
57520-1001	Coumarin	Coumarinum,
63083-1513	Coumarin	Coumarin
44911-0418	Coumarin Phenolic	Coumarinum