FDA.reportPublic FDA data

AMBROSIA ARTEMISIAEFOLIA

Product NDC
60512-6479
11-digit product format
605126479
Labeler code
60512
Product ID
60512-6479_3f54f17f-a819-4667-bbb9-df8ab29aae80
Type
HUMAN OTC DRUG
Nonproprietary name
AMBROSIA ARTEMISIAEFOLIA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
AMBROSIA ARTEMISIIFOLIA
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
60512-6479-12025-12-30C16284748780-19d75b9cf-d43f-f424-e053-dadaa90a57ce5effb2f5-f892-4255-b394-9d7aac4b883e
60512-6479-12020-01-31C16284748780-19d75b9cf-d43f-f424-e053-dadaa90a57ce5effb2f5-f892-4255-b394-9d7aac4b883e

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMBROSIA ARTEMISIIFOLIAACTIVE INGREDIENT9W34L2CQ9AAMBROSIA ARTEMISIAEFOLIA PELLET [HOMEOLAB USA INC.]1
AMBROSIA ARTEMISIIFOLIAACTIVE MOIETY9W34L2CQ9AAMBROSIA ARTEMISIAEFOLIA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAMBROSIA ARTEMISIAEFOLIA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AMBROSIA ARTEMISIAEFOLIA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6479AMBROSIA ARTEMISIAEFOLIA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_5effb2f5-f892-4255-b394-9d7aac4b883e.zip