FDA.reportPublic FDA data

ABROTANUM

Product NDC
60512-6438
11-digit product format
605126438
Labeler code
60512
Product ID
60512-6438_658754ec-2058-474e-be50-213a232a763c
Type
HUMAN OTC DRUG
Nonproprietary name
ABROTANUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ARTEMISIA ABROTANUM 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
60512-6438-12025-12-26C16284748780-19d75b9d0-57b5-f424-e053-dadaa90a57ce6457b1b0-d30d-417b-9d39-66d1e118e979
60512-6438-12020-01-31C16284748780-19d75b9d0-57b5-f424-e053-dadaa90a57ce6457b1b0-d30d-417b-9d39-66d1e118e979

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARTEMISIA ABROTANUM FLOWERING TOPACTIVE INGREDIENTQG07G580U0ABROTANUM PELLET [HOMEOLAB USA INC.]1
ARTEMISIA ABROTANUM FLOWERING TOPACTIVE MOIETYQG07G580U0ABROTANUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GABROTANUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ABROTANUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6438ABROTANUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_6457b1b0-d30d-417b-9d39-66d1e118e979.zip