NDC 63776-653

DHEA

Prasterone

DHEA is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Viatrexx Bio Incorporated. The primary component is Prasterone.

• Product ID: 63776-653_b56d6a23-6a67-4df7-b50d-28f34b0993ea
• NDC: 63776-653
• Product Type: Human Otc Drug
• Proprietary Name: DHEA
• Generic Name: Prasterone
• Dosage Form: Spray
• Route of Administration: ORAL
• Marketing Start Date: 2012-07-24
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: VIATREXX BIO INCORPORATED
• Substance Name: PRASTERONE
• Active Ingredient Strength: 200 [kp_C]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 63776-653-14

1 BOTTLE, SPRAY in 1 BOX (63776-653-14) > 30 mL in 1 BOTTLE, SPRAY

• Marketing Start Date: 2012-07-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63776-653-14 [63776065314]

DHEA SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-24

Drug Details

Active Ingredients

Ingredient	Strength
PRASTERONE	200 [kp_C]/mL

OpenFDA Data

• SPL SET ID: b1971d8f-e72d-96a0-c43f-7ba0103e921e
• Manufacturer:
  • VIATREXX BIO INCORPORATED
• UNII:
  • 459AG36T1B

NDC Crossover Matching brand name "DHEA" or generic name "Prasterone"

NDC	Brand Name	Generic Name
43742-0564	DHEA	DHEA (Dehydroepiandrosterone)
63776-653	DHEA	Prasterone
64011-601	Intrarosa	Prasterone
72495-401	Intrarosa	Prasterone
72495-501	Intrarosa	Prasterone