NDC 43742-0975

Octopamine

Octopamine (hydrochloride)

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

• Product ID: 43742-0975_fa7f6064-adf4-40be-a145-ef0aa0c0cb81
• NDC: 43742-0975
• Product Type: Human Otc Drug
• Proprietary Name: Octopamine
• Generic Name: Octopamine (hydrochloride)
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2017-02-16
• Marketing End Date: 2022-03-16
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: OCTOPAMINE HYDROCHLORIDE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0975-1

30 mL in 1 BOTTLE, DROPPER (43742-0975-1)

• Marketing Start Date: 2017-02-16
• Marketing End Date: 2022-03-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0975-1 [43742097501]

Octopamine LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-02-16
• Marketing End Date: 2022-03-16

Drug Details

Active Ingredients

Ingredient	Strength
OCTOPAMINE HYDROCHLORIDE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 6fb6fdff-fefa-4d33-ba3a-68ac4a840412
• Manufacturer:
  • Deseret Biologicals, 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