NDC 43742-0304

Octopamine

Octopamine

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.

• Product ID: 43742-0304_61f2c44d-f7c7-4a95-82df-742802dd2663
• NDC: 43742-0304
• Product Type: Human Otc Drug
• Proprietary Name: Octopamine
• Generic Name: Octopamine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-01-10
• Marketing End Date: 2019-11-26
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: OCTOPAMINE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0304-1

30 mL in 1 BOTTLE, DROPPER (43742-0304-1)

• Marketing Start Date: 2014-01-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0304-1 [43742030401]

Octopamine LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-10
• Marketing End Date: 2019-11-26

Drug Details

Active Ingredients

Ingredient	Strength
OCTOPAMINE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: aea30147-9167-40b8-83cf-f7c2a2ff80d8
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 14O50WS8JD

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

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