FDA.reportPublic FDA data

ANATHERUM MURICATUM

Product NDC
60512-6489
11-digit product format
605126489
Labeler code
60512
Product ID
60512-6489_ccd29e50-5bf0-496a-bff5-6ea9f954406f
Type
HUMAN OTC DRUG
Nonproprietary name
ANATHERUM MURICATUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CHRYSOPOGON ZIZANIOIDES 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
60512-6489-12025-12-28C16284748780-19d75b9d0-2ac4-f424-e053-dadaa90a57ce6d13ac3b-1ecc-4690-8174-4059b5856392
60512-6489-12020-01-31C16284748780-19d75b9d0-2ac4-f424-e053-dadaa90a57ce6d13ac3b-1ecc-4690-8174-4059b5856392

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHRYSOPOGON ZIZANIOIDES ROOTACTIVE INGREDIENT37TB8LUP9ZANATHERUM MURICATUM PELLET [HOMEOLAB USA INC.]1
CHRYSOPOGON ZIZANIOIDES ROOTACTIVE MOIETY37TB8LUP9ZANATHERUM MURICATUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GANATHERUM MURICATUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ANATHERUM MURICATUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6489ANATHERUM MURICATUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_6d13ac3b-1ecc-4690-8174-4059b5856392.zip