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GELSEMIUM SEMPERVIRENS - 60512-1020-1 - (GELSEMIUM SEMPERVIRENS)

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Drug Information of GELSEMIUM SEMPERVIRENS

Product NDC: 60512-1020
Proprietary Name: GELSEMIUM SEMPERVIRENS
Non Proprietary Name: GELSEMIUM SEMPERVIRENS
Active Ingredient(s): 3    [hp_X]/1 & nbsp;   GELSEMIUM SEMPERVIRENS
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of GELSEMIUM SEMPERVIRENS

Product NDC: 60512-1020
Labeler Name: HOMEOLAB USA INC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19951011

Package Information of GELSEMIUM SEMPERVIRENS

Package NDC: 60512-1020-1
Package Description: 80 PELLET in 1 TUBE (60512-1020-1)

NDC Information of GELSEMIUM SEMPERVIRENS

NDC Code 60512-1020-1
Proprietary Name GELSEMIUM SEMPERVIRENS
Package Description 80 PELLET in 1 TUBE (60512-1020-1)
Product NDC 60512-1020
Product Type Name HUMAN OTC DRUG
Non Proprietary Name GELSEMIUM SEMPERVIRENS
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19951011
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name HOMEOLAB USA INC
Substance Name GELSEMIUM SEMPERVIRENS ROOT
Strength Number 3
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of GELSEMIUM SEMPERVIRENS


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