FDA.reportPublic FDA data

AGAVE AMERICANA

Product NDC
60512-6461
11-digit product format
605126461
Labeler code
60512
Product ID
60512-6461_4c82d2bc-f43c-4cfd-977b-ba3912306d51
Type
HUMAN OTC DRUG
Nonproprietary name
AGAVE AMERICANA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
AGAVE AMERICANA LEAF
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
60512-6461-12025-12-30C16284748780-19d75b9d0-005e-f424-e053-dadaa90a57cebe990687-1357-420f-b437-acc46f223f51
60512-6461-12020-01-31C16284748780-19d75b9d0-005e-f424-e053-dadaa90a57cebe990687-1357-420f-b437-acc46f223f51

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AGAVE AMERICANA LEAFACTIVE INGREDIENT8511ZMP5QKAGAVE AMERICANA PELLET [HOMEOLAB USA INC.]1
AGAVE AMERICANA LEAFACTIVE MOIETY8511ZMP5QKAGAVE AMERICANA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAGAVE AMERICANA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AGAVE AMERICANA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6461AGAVE AMERICANA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_be990687-1357-420f-b437-acc46f223f51.zip