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ANTIMONIUM TARTARICUM - 10191-1841-2 - (ANTIMONY POTASSIUM TARTRATE)

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Drug Information of ANTIMONIUM TARTARICUM

Product NDC: 10191-1841
Proprietary Name: ANTIMONIUM TARTARICUM
Non Proprietary Name: ANTIMONY POTASSIUM TARTRATE
Active Ingredient(s): 6    [hp_C]/1 & nbsp;   ANTIMONY POTASSIUM TARTRATE
Administration Route(s): SUBLINGUAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of ANTIMONIUM TARTARICUM

Product NDC: 10191-1841
Labeler Name: Remedy Makers
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100106

Package Information of ANTIMONIUM TARTARICUM

Package NDC: 10191-1841-2
Package Description: 176 PELLET in 1 VIAL, GLASS (10191-1841-2)

NDC Information of ANTIMONIUM TARTARICUM

NDC Code 10191-1841-2
Proprietary Name ANTIMONIUM TARTARICUM
Package Description 176 PELLET in 1 VIAL, GLASS (10191-1841-2)
Product NDC 10191-1841
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ANTIMONY POTASSIUM TARTRATE
Dosage Form Name PELLET
Route Name SUBLINGUAL
Start Marketing Date 20100106
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Remedy Makers
Substance Name ANTIMONY POTASSIUM TARTRATE
Strength Number 6
Strength Unit [hp_C]/1
Pharmaceutical Classes

Complete Information of ANTIMONIUM TARTARICUM


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