NDC 43742-0955

Levothyroxine

Levothyroxine

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

• Product ID: 43742-0955_7c431149-4f46-4c4f-a5bb-c1b1fb705283
• NDC: 43742-0955
• Product Type: Human Otc Drug
• Proprietary Name: Levothyroxine
• Generic Name: Levothyroxine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2017-01-06
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: LEVOTHYROXINE
• Active Ingredient Strength: 16 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43742-0955-1

30 mL in 1 BOTTLE, DROPPER (43742-0955-1)

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

NDC SPL Data Element Entries

NDC 43742-0955-1 [43742095501]

Levothyroxine LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
LEVOTHYROXINE	16 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 1a467f8b-2611-4936-af2b-098e4791d6ae
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • Q51BO43MG4

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

NDC	Brand Name	Generic Name
43742-0955	Levothyroxine	Levothyroxine
51655-091	Levothyroxine	Levothyroxine
51655-290	LEVOTHYROXINE	LEVOTHYROXINE