NUX VOMICA - 60512-1035-1 - (NUX VOMICA)

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Drug Information of NUX VOMICA

Product NDC: 60512-1035
Proprietary Name: NUX VOMICA
Non Proprietary Name: NUX VOMICA
Active Ingredient(s): 3    [hp_X]/1 & nbsp;   NUX VOMICA
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of NUX VOMICA

Product NDC: 60512-1035
Labeler Name: HOMEOLAB USA INC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19951011

Package Information of NUX VOMICA

Package NDC: 60512-1035-1
Package Description: 80 PELLET in 1 TUBE (60512-1035-1)

NDC Information of NUX VOMICA

NDC Code 60512-1035-1
Proprietary Name NUX VOMICA
Package Description 80 PELLET in 1 TUBE (60512-1035-1)
Product NDC 60512-1035
Product Type Name HUMAN OTC DRUG
Non Proprietary Name NUX VOMICA
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19951011
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name HOMEOLAB USA INC
Substance Name STRYCHNOS NUX-VOMICA SEED
Strength Number 3
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of NUX VOMICA


General Information