FDA.reportPublic FDA data

EUPATORIUM PERFOLIATUM

Product NDC
60512-1017
11-digit product format
605121017
Labeler code
60512
Product ID
60512-1017_aeb4b3a7-164a-4862-83dd-be2aa0d067c0
Type
HUMAN OTC DRUG
Nonproprietary name
EUPATORIUM PERFOLIATUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-18
Marketing end
0000-00-00
Substance
EUPATORIUM PERFOLIATUM FLOWERING TOP
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
60512-1017-12025-12-28C16284748780-19d75b9d1-0dd4-f424-e053-dadaa90a57ce12a2701b-f259-4e7f-a06c-db253ac6db92
60512-1017-12020-01-31C16284748780-19d75b9d1-0dd4-f424-e053-dadaa90a57ce12a2701b-f259-4e7f-a06c-db253ac6db92

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EUPATORIUM PERFOLIATUM FLOWERING TOPACTIVE INGREDIENT1W0775VX6EEUPATORIUM PERFOLIATUM PELLET [HOMEOLAB USA INC.]1
EUPATORIUM PERFOLIATUM FLOWERING TOPACTIVE MOIETY1W0775VX6EEUPATORIUM PERFOLIATUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GEUPATORIUM PERFOLIATUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554EUPATORIUM PERFOLIATUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1017EUPATORIUM PERFOLIATUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20140426_12a2701b-f259-4e7f-a06c-db253ac6db92.zip