FDA.reportPublic FDA data

ASAFOETIDA

Product NDC
60512-6522
11-digit product format
605126522
Labeler code
60512
Product ID
60512-6522_a09236ca-b811-4f5e-a8a5-7144af001b79
Type
HUMAN OTC DRUG
Nonproprietary name
ASAFOETIDA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ASAFETIDA
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
60512-6522-12025-12-28C16284748780-19d75b9d0-e134-f424-e053-dadaa90a57ce943ce71e-613b-42ae-a10e-fd34d67f9ca9
60512-6522-12020-01-31C16284748780-19d75b9d0-e134-f424-e053-dadaa90a57ce943ce71e-613b-42ae-a10e-fd34d67f9ca9

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ASAFETIDAACTIVE INGREDIENTW9FZA51AS1ASAFOETIDA PELLET [HOMEOLAB USA INC.]1
ASAFETIDAACTIVE MOIETYW9FZA51AS1ASAFOETIDA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GASAFOETIDA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ASAFOETIDA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6522ASAFOETIDA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131030_943ce71e-613b-42ae-a10e-fd34d67f9ca9.zip