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Fibro Relief - 57520-0272-1 - (Ferrum metallicum, Guaiacum, Lithium carbonicum, Lycopersicum esculentum, Magnesia phosphorica)

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Drug Information of Fibro Relief

Product NDC: 57520-0272
Proprietary Name: Fibro Relief
Non Proprietary Name: Ferrum metallicum, Guaiacum, Lithium carbonicum, Lycopersicum esculentum, Magnesia phosphorica
Active Ingredient(s): 30; 30; 30; 30; 30    [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp;   Ferrum metallicum, Guaiacum, Lithium carbonicum, Lycopersicum esculentum, Magnesia phosphorica
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fibro Relief

Product NDC: 57520-0272
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20101217

Package Information of Fibro Relief

Package NDC: 57520-0272-1
Package Description: 120 CAPSULE in 1 BOTTLE (57520-0272-1)

NDC Information of Fibro Relief

NDC Code 57520-0272-1
Proprietary Name Fibro Relief
Package Description 120 CAPSULE in 1 BOTTLE (57520-0272-1)
Product NDC 57520-0272
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ferrum metallicum, Guaiacum, Lithium carbonicum, Lycopersicum esculentum, Magnesia phosphorica
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101217
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name GUAIACUM OFFICINALE RESIN; IRON; LITHIUM CARBONATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; TOMATO
Strength Number 30; 30; 30; 30; 30
Strength Unit [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
Pharmaceutical Classes

Complete Information of Fibro Relief


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