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Name:Apomorphinum Muriaticum
Manufacturer:Remedy Makers
Category:Homeopathic Marketed Drugs


APOMORPHINUM MURIATICUM 3X (Apomorphine Hydrochloride)

APOMORPHINUM MURIATICUM  - apomorphine hydrochloride pellet 
Remedy Makers

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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APOMORPHINUM MURIATICUM 3X (Apomorphine Hydrochloride)

Free from yeast, wheat, corn, and soy.
DIRECTIONS: Dissolve 3 or 4 pellets
in mouth or under tongue 3 times a day or as directed by a physician.
Children 2 years and older take 1/2
adult dose.
INDICATIONS: To be used according
to standard homeopathic indications
for self limiting conditions such as
those indicated on the front panel or as directed by a physician.
Warnings: *Use only if cap and
seal are unbroken. * Keep this and all medications out of reach of children.
* If symptoms persist for more then 3
days, consult your physician.
*As with any drug, if your are pregnant or nursing a baby, seek the advice of a
health professional before using this product.*Store tightly closed in a cool, dark place.
Made according to The Homoeopathic Pharmacopoeia of the United States by: Remedy Makers, Pomona, CA 91768

Image of APOMORPHINUM MURIATICUM vial glass labelEnter section text here


APOMORPHINUM MURIATICUM 
apomorphine hydrochloride pellet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10191-1225
Route of Administration SUBLINGUAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
APOMORPHINE HYDROCHLORIDE (APOMORPHINE ) APOMORPHINE HYDROCHLORIDE 3 [hp_X]
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:10191-1225-2 153 PELLET ( PELLET) in 1 VIAL, GLASS None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 03/18/2002

Labeler - Remedy Makers (018543582)

Revised: 12/2009 Remedy Makers



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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