Aurum 10X

Product NDC
48951-1349
Requested package NDC
48951-1349-1
11-digit product format
489511349
Labeler code
48951
Product ID
48951-1349_c706aaf0-a97b-7848-e053-2995a90a0aca
Type
HUMAN OTC DRUG
Nonproprietary name
Aurum 10X
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
GOLD
Active strength
10 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage48951-134948951-1349-1IInactivated by FDA2026-08-11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1349-1Aurum 10X1 mL in 1 AMPULELIQUID11
48951-1349-1Aurum 10X10 in 1 BOXLIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1349AURUM 10X LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 2 package rows20210714_c706aaf0-a97a-7848-e053-2995a90a0aca.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1349-14895113490110 AMPULE in 1 BOX (48951-1349-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent