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Depressoforce - 57520-0080-1 - (Depressoforce)

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Drug Information of Depressoforce

Product NDC: 57520-0080
Proprietary Name: Depressoforce
Non Proprietary Name: Depressoforce
Active Ingredient(s): 30; 30; 30; 30; 30; 30; 30; 12    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Depressoforce
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Depressoforce

Product NDC: 57520-0080
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100210

Package Information of Depressoforce

Package NDC: 57520-0080-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0080-1)

NDC Information of Depressoforce

NDC Code 57520-0080-1
Proprietary Name Depressoforce
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0080-1)
Product NDC 57520-0080
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Depressoforce
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100210
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name ARSENIC TRIOXIDE; GOLD; NITRIC ACID; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; STRYCHNOS IGNATII SEED; TRINITROPHENOL
Strength Number 30; 30; 30; 30; 30; 30; 30; 12
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Depressoforce


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