FDA.reportPublic FDA data

ANILINUM

Product NDC
60512-6180
11-digit product format
605126180
Labeler code
60512
Product ID
60512-6180_6393da1d-5b31-4974-9c36-cab67cadec8d
Type
HUMAN OTC DRUG
Nonproprietary name
ANILINUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ANILINE
Active strength
4 [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
60512-6180-12025-12-29C16284748780-19d75b9d0-2ac7-f424-e053-dadaa90a57ce8e451a06-8b2b-42c9-988a-00af44886b83
60512-6180-12020-01-31C16284748780-19d75b9d0-2ac7-f424-e053-dadaa90a57ce8e451a06-8b2b-42c9-988a-00af44886b83

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANILINEACTIVE INGREDIENTSIR7XX2F1KANILINUM PELLET [HOMEOLAB USA INC.]1
ANILINEACTIVE MOIETYSIR7XX2F1KANILINUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GANILINUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ANILINUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6180ANILINUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_8e451a06-8b2b-42c9-988a-00af44886b83.zip