FDA.reportPublic FDA data

ALETRIS FARINOSA

Product NDC
60512-6468
11-digit product format
605126468
Labeler code
60512
Product ID
60512-6468_e9917566-8144-4222-9409-308b09ebd5ca
Type
HUMAN OTC DRUG
Nonproprietary name
ALETRIS FARINOSA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ALETRIS FARINOSA ROOT
Active strength
1 [hp_X]/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-6468-12025-12-28C16284748780-19d75b9d0-0052-f424-e053-dadaa90a57ce43ee58a3-cd93-40dd-94ce-4217e6e1a5fd
60512-6468-12020-01-31C16284748780-19d75b9d0-0052-f424-e053-dadaa90a57ce43ee58a3-cd93-40dd-94ce-4217e6e1a5fd

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALETRIS FARINOSA ROOTACTIVE INGREDIENTO021JGR97XALETRIS FARINOSA PELLET [HOMEOLAB USA INC.]1
ALETRIS FARINOSA ROOTACTIVE MOIETYO021JGR97XALETRIS FARINOSA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALETRIS FARINOSA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALETRIS FARINOSA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6468ALETRIS FARINOSA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_43ee58a3-cd93-40dd-94ce-4217e6e1a5fd.zip