FDA.reportPublic FDA data

PHOSPHORUS

Product NDC
60512-1036
11-digit product format
605121036
Labeler code
60512
Product ID
60512-1036_9ba663c8-3830-49dd-8cd9-4de2d30983a8
Type
HUMAN OTC DRUG
Nonproprietary name
PHOSPHORUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-15
Marketing end
0000-00-00
Substance
PHOSPHORUS
Active strength
4 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1036-12025-12-28C16284748780-19d75b9d0-00be-f424-e053-dadaa90a57ce4a15da0a-adde-47b5-835a-ad47ba4f8665
60512-1036-12020-01-31C16284748780-19d75b9d0-00be-f424-e053-dadaa90a57ce4a15da0a-adde-47b5-835a-ad47ba4f8665

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PHOSPHORUSACTIVE INGREDIENT27YLU75U4WPHOSPHORUS PELLET [HOMEOLAB USA INC]1
PHOSPHORUSACTIVE MOIETY27YLU75U4WPHOSPHORUS PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GPHOSPHORUS PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554PHOSPHORUS PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1036PHOSPHORUS PELLET [HOMEOLAB USA INC]1Legacy NDC20111207_4a15da0a-adde-47b5-835a-ad47ba4f8665.zip