Adrenoplex - 57520-0018-1 - (Chelidonium majus, Echinacea angustifolia)

Alphabetical Index


Drug Information of Adrenoplex

Product NDC: 57520-0018
Proprietary Name: Adrenoplex
Non Proprietary Name: Chelidonium majus, Echinacea angustifolia
Active Ingredient(s): 8; 3; 3; 12; 12; 12; 12; 8    [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;   Chelidonium majus, Echinacea angustifolia
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Adrenoplex

Product NDC: 57520-0018
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100128

Package Information of Adrenoplex

Package NDC: 57520-0018-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0018-1)

NDC Information of Adrenoplex

NDC Code 57520-0018-1
Proprietary Name Adrenoplex
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0018-1)
Product NDC 57520-0018
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chelidonium majus, Echinacea angustifolia
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100128
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name BOS TAURUS ADRENAL GLAND; CHELIDONIUM MAJUS; ECHINACEA ANGUSTIFOLIA; LYCOPODIUM CLAVATUM SPORE; PHOSPHORIC ACID; SILYBUM MARIANUM SEED; SODIUM CHLORIDE; SUS SCROFA SPLEEN
Strength Number 8; 3; 3; 12; 12; 12; 12; 8
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 Adrenoplex


General Information