NDC 57520-1001

Coumarin

Coumarinum,

Coumarin is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Apotheca Company. The primary component is Coumarin.

• Product ID: 57520-1001_15438445-fcd3-4ce7-a6ad-f88d9102bda8
• NDC: 57520-1001
• Product Type: Human Otc Drug
• Proprietary Name: Coumarin
• Generic Name: Coumarinum,
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2011-12-15
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Apotheca Company
• Substance Name: COUMARIN
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 57520-1001-1

30 mL in 1 BOTTLE, DROPPER (57520-1001-1)

• Marketing Start Date: 2011-12-15
• Marketing End Date: 2022-11-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 57520-1001-1 [57520100101]

Coumarin LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-15
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
COUMARIN	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 638f5a02-0f10-4cbc-87f8-5b5d4fef209b
• Manufacturer:
  • Apotheca Company
• 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