FDA.reportPublic FDA data

AMMONIUM MURIATICUM

Product NDC
60512-6171
11-digit product format
605126171
Labeler code
60512
Product ID
60512-6171_9c42283b-af8f-46d6-b824-c3c26167064e
Type
HUMAN OTC DRUG
Nonproprietary name
AMMONIUM MURIATICUM
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 CHLORIDE
Active strength
1 [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
60512-6171-12025-12-30C16284748780-19d75b9cf-fff8-f424-e053-dadaa90a57cec70b4744-31c6-4d8a-b133-124c061df8dd
60512-6171-12020-01-31C16284748780-19d75b9cf-fff8-f424-e053-dadaa90a57cec70b4744-31c6-4d8a-b133-124c061df8dd

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMMONIUM CHLORIDEACTIVE INGREDIENT01Q9PC255DAMMONIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1
AMMONIUM CATIONACTIVE MOIETY54S68520I4AMMONIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAMMONIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AMMONIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6171AMMONIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_c70b4744-31c6-4d8a-b133-124c061df8dd.zip