FDA.reportPublic FDA data

ANGUSTURA VERA

Product NDC
60512-6497
11-digit product format
605126497
Labeler code
60512
Product ID
60512-6497_f793144f-441c-4d0c-be63-2a5cfd3d972b
Type
HUMAN OTC DRUG
Nonproprietary name
ANGUSTURA VERA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ANGOSTURA BARK
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
60512-6497-12025-12-30C16284748780-19d75b9cf-d451-f424-e053-dadaa90a57ce4b9dc68a-9811-445f-a405-da2f5e1f05eb
60512-6497-12020-01-31C16284748780-19d75b9cf-d451-f424-e053-dadaa90a57ce4b9dc68a-9811-445f-a405-da2f5e1f05eb

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANGOSTURA BARKACTIVE INGREDIENT104010O5VUANGUSTURA VERA PELLET [HOMEOLAB USA INC.]1
ANGOSTURA BARKACTIVE MOIETY104010O5VUANGUSTURA VERA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GANGUSTURA VERA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ANGUSTURA VERA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6497ANGUSTURA VERA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_4b9dc68a-9811-445f-a405-da2f5e1f05eb.zip