APOMORPHINUM MURIATICUM

Manufacturer
Remedy Makers
Effective date
2009-12-30
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:02:07

Label at a glance#

ProductAPOMORPHINUM MURIATICUM
Active ingredientAPOMORPHINE HYDROCHLORIDE
Label structure2 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of APOMORPHINUM MURIATICUM vial glass labelImage of APOMORPHINUM MURIATICUM vial glass labelEnter section text here

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8cacec2b-1363-4e94-885c-4189d5e7208aProduct name120251117
d7fea1a2-3459-27e8-1231-1b79988f4937Product name220221207
3a53909e-cbfb-4956-984e-a33101906fd9Product name120201021

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10191-1225-22019-10-21C16284748780-1956f9ecf-ce19-621f-e053-dbdaa90a74adAPOMORPHINUM MURIATICUM 3X (Apomorphine Hydrochloride)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10191-1225-2APOMORPHINUM MURIATICUM153 in 1 VIAL, GLASSPELLET1536

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10191-1225APOMORPHINUM MURIATICUM (APOMORPHINE HYDROCHLORIDE) PELLET [REMEDY MAKERS]6Legacy NDC, 1 package rows20091231_72093a71-cada-44bc-985e-51e30fd91a1a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
APOMORPHINE HYDROCHLORIDEACTIVE INGREDIENTF39049Y0686
APOMORPHINEACTIVE MOIETYN21FAR7B4S6

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10191-122510191-1225-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
APOMORPHINE HYDROCHLORIDEF39049Y068ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1cd90a1d-3598-4430-b7b6-e5406454b2c972093a71-cada-44bc-985e-51e30fd91a1a2009-12-30Exact identifier
spl id: 1cd90a1d-3598-4430-b7b6-e5406454b2c9
spl set id: 72093a71-cada-44bc-985e-51e30fd91a1a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.