FDA.reportPublic FDA data

ALFALFA

Product NDC
60512-6469
11-digit product format
605126469
Labeler code
60512
Product ID
60512-6469_10c1ea72-3eaf-44b1-8639-4c1aded50551
Type
HUMAN OTC DRUG
Nonproprietary name
ALFALFA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ALFALFA WHOLE
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
60512-6469-12025-12-28C16284748780-19d75b9d1-079e-f424-e053-dadaa90a57ce8b6756cf-46c2-4005-95cd-3ef657f4750d
60512-6469-12020-01-31C16284748780-19d75b9d1-079e-f424-e053-dadaa90a57ce8b6756cf-46c2-4005-95cd-3ef657f4750d

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALFALFA WHOLEACTIVE INGREDIENTDJO934BRBDALFALFA PELLET [HOMEOLAB USA INC.]1
ALFALFAACTIVE MOIETYDJO934BRBDALFALFA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALFALFA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALFALFA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6469ALFALFA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_8b6756cf-46c2-4005-95cd-3ef657f4750d.zip