FDA.reportPublic FDA data

APIUM GRAVEOLENS

Product NDC
60512-6502
11-digit product format
605126502
Labeler code
60512
Product ID
60512-6502_d1b868c8-b10f-450d-b3f7-3ad65b4b2ec5
Type
HUMAN OTC DRUG
Nonproprietary name
APIUM GRAVEOLENS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CELERY SEED
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
60512-6502-12025-12-29C16284748780-19d75b9d1-0735-f424-e053-dadaa90a57cea5770bc4-7776-42eb-ab18-560c6d262672
60512-6502-12020-01-31C16284748780-19d75b9d1-0735-f424-e053-dadaa90a57cea5770bc4-7776-42eb-ab18-560c6d262672

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CELERY SEEDACTIVE INGREDIENT1G1EAA320LAPIUM GRAVEOLENS PELLET [HOMEOLAB USA INC.]1
CELERY SEEDACTIVE MOIETY1G1EAA320LAPIUM GRAVEOLENS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAPIUM GRAVEOLENS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554APIUM GRAVEOLENS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6502APIUM GRAVEOLENS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131030_a5770bc4-7776-42eb-ab18-560c6d262672.zip