FDA.reportPublic FDA data

ADRENOCORTICOTROPHIN

Product NDC
60512-6158
11-digit product format
605126158
Labeler code
60512
Product ID
60512-6158_f0c6c22e-405e-4840-8696-e28246cee59d
Type
HUMAN OTC DRUG
Nonproprietary name
ADRENOCORTICOTROPHIN
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CORTICOTROPIN
Active strength
6 [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
60512-6158-12025-12-27C16284748780-19d75b9d0-2b2d-f424-e053-dadaa90a57ce7cc94bcb-115c-4e27-b463-e1ecee300513
60512-6158-12020-01-31C16284748780-19d75b9d0-2b2d-f424-e053-dadaa90a57ce7cc94bcb-115c-4e27-b463-e1ecee300513

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CORTICOTROPINACTIVE INGREDIENTK0U68Q2TXAADRENOCORTICOTROPHIN PELLET [HOMEOLAB USA INC.]1
CORTICOTROPINACTIVE MOIETYK0U68Q2TXAADRENOCORTICOTROPHIN PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GADRENOCORTICOTROPHIN PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ADRENOCORTICOTROPHIN PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6158ADRENOCORTICOTROPHIN PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_7cc94bcb-115c-4e27-b463-e1ecee300513.zip