Ferrum 12X

Product NDC
48951-4157
11-digit product format
489514157
Labeler code
48951
Product ID
48951-4157_940612af-ec33-09f6-e053-2a95a90a6641
Type
HUMAN OTC DRUG
Nonproprietary name
Ferrum 12X
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
IRON
Active strength
12 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-4157-12026-01-29C16284748780-149896155-a4d8-586f-e063-e6dba90add90Ferrum 12X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4157-1Ferrum 12X60 mL in 1 BOTTLE, DROPPERLIQUID603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4157FERRUM 12X LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 1 package rows20241208_940612af-ec32-09f6-e053-2a95a90a6641.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4157-14895141570160 mL in 1 BOTTLE, DROPPER (48951-4157-1) 60 ml2009-09-010000-00-00NoNoCurrent