FDA.reportPublic FDA data

AMMONIUM PHOSPHORICUM

Product NDC
60512-6173
11-digit product format
605126173
Labeler code
60512
Product ID
60512-6173_95763f2e-79ff-410b-8ef9-caeac33b2029
Type
HUMAN OTC DRUG
Nonproprietary name
AMMONIUM PHOSPHORICUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
AMMONIUM PHOSPHATE, DIBASIC
Active strength
3 [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
60512-6173-12025-12-28C16284748780-19d75b9d0-aff0-f424-e053-dadaa90a57ce0b2fa879-b722-466a-81ae-f0aa5c7efe3b
60512-6173-12020-01-31C16284748780-19d75b9d0-aff0-f424-e053-dadaa90a57ce0b2fa879-b722-466a-81ae-f0aa5c7efe3b

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMMONIUM PHOSPHATE, DIBASICACTIVE INGREDIENT10LGE70FSUAMMONIUM PHOSPHORICUM PELLET [HOMEOLAB USA INC.]1
PHOSPHATE IONACTIVE MOIETYNK08V8K8HRAMMONIUM PHOSPHORICUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAMMONIUM PHOSPHORICUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AMMONIUM PHOSPHORICUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6173AMMONIUM PHOSPHORICUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_0b2fa879-b722-466a-81ae-f0aa5c7efe3b.zip