NDC 43742-0211

Rutin

Rutin

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

• Product ID: 43742-0211_228e991c-64c2-4cd8-a7c6-1507ea8101f5
• NDC: 43742-0211
• Product Type: Human Otc Drug
• Proprietary Name: Rutin
• Generic Name: Rutin
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2012-02-27
• Marketing End Date: 2022-06-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: RUTIN
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0211-1

30 mL in 1 BOTTLE, DROPPER (43742-0211-1)

• Marketing Start Date: 2017-04-26
• Marketing End Date: 2022-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0211-1 [43742021101]

Rutin LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-04-26
• Marketing End Date: 2022-06-01

Drug Details

Active Ingredients

Ingredient	Strength
RUTIN	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 4ccdad7d-22ab-426e-b222-0f11a42af56b
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 5G06TVY3R7

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

NDC	Brand Name	Generic Name
43742-0211	Rutin	Rutin
43857-0264	RUTIN	not applicable
63083-1541	Rutin	Rutin