FDA.reportPublic FDA data

AMBRA GRISEA

Product NDC
60512-7101
11-digit product format
605127101
Labeler code
60512
Product ID
60512-7101_cafb8adf-a8f6-46f1-8183-552091dffe21
Type
HUMAN OTC DRUG
Nonproprietary name
AMBRA GRISEA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
AMBERGRIS
Active strength
2 [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
60512-7101-12025-12-29C16284748780-19d75b9cf-d442-f424-e053-dadaa90a57ce74c58419-30be-4d7d-993c-bd06e2de3578
60512-7101-12020-01-31C16284748780-19d75b9cf-d442-f424-e053-dadaa90a57ce74c58419-30be-4d7d-993c-bd06e2de3578

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMBERGRISACTIVE INGREDIENTXTC0D02P6CAMBRA GRISEA PELLET [HOMEOLAB USA INC.]1
AMBERGRISACTIVE MOIETYXTC0D02P6CAMBRA GRISEA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAMBRA GRISEA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AMBRA GRISEA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-7101AMBRA GRISEA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_74c58419-30be-4d7d-993c-bd06e2de3578.zip