FDA.reportPublic FDA data

DIGITALIS PURPUREA

Product NDC
60512-6643
11-digit product format
605126643
Labeler code
60512
Product ID
60512-6643_b428c3f0-14c5-441d-a208-d39d3ad9e236
Type
HUMAN OTC DRUG
Nonproprietary name
DIGITALIS PURPUREA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-18
Marketing end
0000-00-00
Substance
DIGITALIS
Active strength
8 [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
60512-6643-12025-12-29C16284748780-19d75b9d0-7c4b-f424-e053-dadaa90a57ce60d720e1-1110-4f2b-85fe-2f5346e3a450
60512-6643-12020-01-31C16284748780-19d75b9d0-7c4b-f424-e053-dadaa90a57ce60d720e1-1110-4f2b-85fe-2f5346e3a450

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DIGITALISACTIVE INGREDIENTF1T8QT9U8BDIGITALIS PURPUREA PELLET [HOMEOLAB USA INC.]1
DIGITALISACTIVE MOIETYF1T8QT9U8BDIGITALIS PURPUREA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GDIGITALIS PURPUREA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554DIGITALIS PURPUREA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6643DIGITALIS PURPUREA PELLET [HOMEOLAB USA INC.]1Legacy NDC20140513_60d720e1-1110-4f2b-85fe-2f5346e3a450.zip