GRAPHITES

Product NDC
10191-1797
11-digit product format
101911797
Labeler code
10191
Product ID
10191-1797_5cca3e35-d449-4dbd-b47f-f6be94098451
Type
HUMAN OTC DRUG
Nonproprietary name
GRAPHITE
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
Remedy Makers
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2004-10-14
Marketing end
0000-00-00
Substance
GRAPHITE
Active strength
30 [hp_C]/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10191-1797-22019-10-21C16284748780-1956f9ecf-c21f-621f-e053-dbdaa90a74adGRAPHITES 30C (Graphite)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10191-1797-2GRAPHITES175 in 1 VIAL, GLASSPELLET1751

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GRAPHITEACTIVE INGREDIENT4QQN74LH4OGRAPHITES (GRAPHITE) PELLET [REMEDY MAKERS]1
GRAPHITEACTIVE MOIETY4QQN74LH4OGRAPHITES (GRAPHITE) PELLET [REMEDY MAKERS]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10191-1797GRAPHITES (GRAPHITE) PELLET [REMEDY MAKERS]1Legacy NDC, 1 package rows20100225_e4cedd9f-02d9-46d1-80ae-f1de2dbdefe8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
10191-1797-210191179702175 in 1 VIAL, GLASSHistorical