FDA.reportPublic FDA data

ANTIMONIUM TARTARICUM

Product NDC
60512-1004
11-digit product format
605121004
Labeler code
60512
Product ID
60512-1004_38c308cc-916f-49d6-9fa1-8c5f8f6caeb7
Type
HUMAN OTC DRUG
Nonproprietary name
ANTIMONIUM TARTARICUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ANTIMONY POTASSIUM TARTRATE
Active strength
3 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1004-12025-12-29C16284748780-19d75b9d0-c2f5-f424-e053-dadaa90a57ce4877b0af-7bc3-44ac-b50b-363903c9d1d3
60512-1004-12020-01-31C16284748780-19d75b9d0-c2f5-f424-e053-dadaa90a57ce4877b0af-7bc3-44ac-b50b-363903c9d1d3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANTIMONY POTASSIUM TARTRATEACTIVE INGREDIENTDL6OZ476V3ANTIMONIUM TARTARICUM PELLET [HOMEOLAB USA INC]1
ANTIMONY CATION (3+)ACTIVE MOIETY069647RPT5ANTIMONIUM TARTARICUM PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GANTIMONIUM TARTARICUM PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554ANTIMONIUM TARTARICUM PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1004ANTIMONIUM TARTARICUM PELLET [HOMEOLAB USA INC]1Legacy NDC20111202_4877b0af-7bc3-44ac-b50b-363903c9d1d3.zip