"57520-0082-1" National Drug Code (NDC)

NDC Code	57520-0082-1
Package Description	30 mL in 1 BOTTLE (57520-0082-1)
Product NDC	57520-0082
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Dhea Forte
Non-Proprietary Name	Dehydroepiandrosterone (dhea), Pregnenolone, Progesterone,
Dosage Form	SPRAY
Usage	ORAL
Start Marketing Date	20100211
End Marketing Date	20170109
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Apotheca, Inc.
Substance Name	PRASTERONE; PREGNENOLONE; PROGESTERONE
Strength	6; 6; 6
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL