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Bio Clematis - 57520-0009-1 - (Clematis)

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Drug Information of Bio Clematis

Product NDC: 57520-0009
Proprietary Name: Bio Clematis
Non Proprietary Name: Clematis
Active Ingredient(s): 200    [hp_C]/mL & nbsp;   Clematis
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Bio Clematis

Product NDC: 57520-0009
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100203

Package Information of Bio Clematis

Package NDC: 57520-0009-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0009-1)

NDC Information of Bio Clematis

NDC Code 57520-0009-1
Proprietary Name Bio Clematis
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0009-1)
Product NDC 57520-0009
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Clematis
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100203
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name CLEMATIS VITALBA FLOWER
Strength Number 200
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of Bio Clematis


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