NDC 43742-0564

DHEA

Dhea (dehydroepiandrosterone)

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

• Product ID: 43742-0564_93907d1e-db5d-4043-aa36-6070eb16180b
• NDC: 43742-0564
• Product Type: Human Otc Drug
• Proprietary Name: DHEA
• Generic Name: Dhea (dehydroepiandrosterone)
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-01-19
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: PRASTERONE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 43742-0564-1

30 mL in 1 BOTTLE, DROPPER (43742-0564-1)

• Marketing Start Date: 2015-01-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0564-1 [43742056401]

DHEA LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-01-19

Drug Details

Active Ingredients

Ingredient	Strength
PRASTERONE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: d6edd874-495c-4eb5-bf3d-72c2ee41fc88
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 459AG36T1B

NDC Crossover Matching brand name "DHEA" or generic name "Dhea (dehydroepiandrosterone)"

NDC	Brand Name	Generic Name
43742-0564	DHEA	DHEA (Dehydroepiandrosterone)
63776-653	DHEA	Prasterone