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ANTIMONIUM TARTARICUM - 60512-1004-1 - (ANTIMONIUM TARTARICUM)

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Drug Information of ANTIMONIUM TARTARICUM

Product NDC: 60512-1004
Proprietary Name: ANTIMONIUM TARTARICUM
Non Proprietary Name: ANTIMONIUM TARTARICUM
Active Ingredient(s): 3    [hp_X]/1 & nbsp;   ANTIMONIUM TARTARICUM
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of ANTIMONIUM TARTARICUM

Product NDC: 60512-1004
Labeler Name: HOMEOLAB USA INC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19951011

Package Information of ANTIMONIUM TARTARICUM

Package NDC: 60512-1004-1
Package Description: 80 PELLET in 1 TUBE (60512-1004-1)

NDC Information of ANTIMONIUM TARTARICUM

NDC Code 60512-1004-1
Proprietary Name ANTIMONIUM TARTARICUM
Package Description 80 PELLET in 1 TUBE (60512-1004-1)
Product NDC 60512-1004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ANTIMONIUM TARTARICUM
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19951011
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name HOMEOLAB USA INC
Substance Name ANTIMONY POTASSIUM TARTRATE
Strength Number 3
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of ANTIMONIUM TARTARICUM


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