Aurum Stibium

Product NDC
48951-1346
11-digit product format
489511346
Labeler code
48951
Product ID
48951-1346_48871cbc-a3b4-388c-e063-6394a90a3013
Type
HUMAN OTC DRUG
Nonproprietary name
Aurum Stibium
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ANTIMONY; GOLD
Active strength
8; 10 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Aurum Stibium
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANTIMONY8 [hp_X]/mL
GOLD10 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9IT35J3UV3, 79Y1949PYO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1346-1Aurum Stibium1 mL in 1 AMPULELIQUID12
48951-1346-1Aurum Stibium10 in 1 BOXLIQUID102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1346AURUM STIBIUM LIQUID [URIEL PHARMACY INC.]1Current NDC, Legacy NDC, 2 package rows20210312_bd35c88f-c646-4136-e053-2a95a90a0cc1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1346-14895113460110 AMPULE in 1 BOX (48951-1346-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent