NDC 43857-0503

Octopamine

Octopamine Hydrochloride

Octopamine is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritional, Inc.. The primary component is Octopamine Hydrochloride.

• Product ID: 43857-0503_743cc334-e300-4001-a2cc-c481eb87918a
• NDC: 43857-0503
• Product Type: Human Otc Drug
• Proprietary Name: Octopamine
• Generic Name: Octopamine Hydrochloride
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2019-01-09
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: BioActive Nutritional, Inc.
• Substance Name: OCTOPAMINE HYDROCHLORIDE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43857-0503-1

30 mL in 1 BOTTLE, DROPPER (43857-0503-1)

• Marketing Start Date: 2019-01-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43857-0503-1 [43857050301]

Octopamine LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-01-09

Drug Details

Active Ingredients

Ingredient	Strength
OCTOPAMINE HYDROCHLORIDE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 77efc2ee-a59f-4bb2-956b-82762fe256a8
• Manufacturer:
  • BioActive Nutritional, Inc.
• UNII:
  • 37YAS5L9HQ

NDC Crossover Matching brand name "Octopamine" or generic name "Octopamine Hydrochloride"

NDC	Brand Name	Generic Name
43742-0304	Octopamine	Octopamine
43742-0975	Octopamine	Octopamine (Hydrochloride)
43857-0503	Octopamine	Octopamine Hydrochloride
63083-1531	Octopamine	Octopamine