NDC 43742-0245

Piperine

Piperine

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

• Product ID: 43742-0245_9652d021-8970-4823-91f2-d696f045f762
• NDC: 43742-0245
• Product Type: Human Prescription Drug
• Proprietary Name: Piperine
• Generic Name: Piperine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-08-09
• Marketing End Date: 2021-01-20
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: PIPERINE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0245-1

30 mL in 1 PACKAGE (43742-0245-1)

• Marketing Start Date: 2013-08-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0245-1 [43742024501]

Piperine LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-08-09
• Marketing End Date: 2021-01-20

Drug Details

Active Ingredients

Ingredient	Strength
PIPERINE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 6cbe4864-5174-4365-af07-88b1eb24b1c2
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • U71XL721QK

NDC Crossover Matching brand name "Piperine" or generic name "Piperine"

NDC	Brand Name	Generic Name
43742-0245	Piperine	Piperine
57520-1002	Piperine	Piperine,
63083-1537	Piperine	Piperine