FDA.reportPublic FDA data

BELLADONNA

Product NDC
60512-1006
11-digit product format
605121006
Labeler code
60512
Product ID
60512-1006_69d77078-dcce-44c5-8616-9df1c0a1a7b5
Type
HUMAN OTC DRUG
Nonproprietary name
BELLADONNA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ATROPA BELLADONNA
Active strength
3 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1006-12025-12-28C16284748780-19d75b9d0-d04e-f424-e053-dadaa90a57ce962b8ddf-3265-430c-ac73-cf50aae76601
60512-1006-12020-01-31C16284748780-19d75b9d0-d04e-f424-e053-dadaa90a57ce962b8ddf-3265-430c-ac73-cf50aae76601

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0HBELLADONNA PELLET [HOMEOLAB USA INC]1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0HBELLADONNA PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GBELLADONNA PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554BELLADONNA PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1006BELLADONNA PELLET [HOMEOLAB USA INC]1Legacy NDC20111202_962b8ddf-3265-430c-ac73-cf50aae76601.zip