FDA.reportPublic FDA data

AMYL NITROSUM

Product NDC
60512-6179
11-digit product format
605126179
Labeler code
60512
Product ID
60512-6179_2dec9d72-244b-4ff0-b11f-6d8d70d9d959
Type
HUMAN OTC DRUG
Nonproprietary name
AMYL NITROSUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
AMYL NITRITE
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
60512-6179-12025-12-29C16284748780-19d75b9d0-4fae-f424-e053-dadaa90a57ce59b5e194-3bfe-4920-9e9e-49826afe0f6c
60512-6179-12020-01-31C16284748780-19d75b9d0-4fae-f424-e053-dadaa90a57ce59b5e194-3bfe-4920-9e9e-49826afe0f6c

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMYL NITRITEACTIVE INGREDIENT22T8Z09XAKAMYL NITROSUM PELLET [HOMEOLAB USA INC.]2
AMYL NITRITEACTIVE MOIETY22T8Z09XAKAMYL NITROSUM PELLET [HOMEOLAB USA INC.]2
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAMYL NITROSUM PELLET [HOMEOLAB USA INC.]2
SUCROSEINACTIVE INGREDIENTC151H8M554AMYL NITROSUM PELLET [HOMEOLAB USA INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6179AMYL NITROSUM PELLET [HOMEOLAB USA INC.]2Legacy NDC20140515_59b5e194-3bfe-4920-9e9e-49826afe0f6c.zip