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ANTIMONIUM CRUDUM - 60512-1003-1 - (ANTIMONIUM CRUDUM)

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Drug Information of ANTIMONIUM CRUDUM

Product NDC: 60512-1003
Proprietary Name: ANTIMONIUM CRUDUM
Non Proprietary Name: ANTIMONIUM CRUDUM
Active Ingredient(s): 3    [hp_X]/1 & nbsp;   ANTIMONIUM CRUDUM
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of ANTIMONIUM CRUDUM

Product NDC: 60512-1003
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 CRUDUM

Package NDC: 60512-1003-1
Package Description: 80 PELLET in 1 TUBE (60512-1003-1)

NDC Information of ANTIMONIUM CRUDUM

NDC Code 60512-1003-1
Proprietary Name ANTIMONIUM CRUDUM
Package Description 80 PELLET in 1 TUBE (60512-1003-1)
Product NDC 60512-1003
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ANTIMONIUM CRUDUM
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19951011
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name HOMEOLAB USA INC
Substance Name ANTIMONY TRISULFIDE
Strength Number 3
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of ANTIMONIUM CRUDUM


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