Plumbum 8X

Product NDC
48951-8362
11-digit product format
489518362
Labeler code
48951
Product ID
48951-8362_994b027a-d7d3-7fb1-e053-2a95a90a3f96
Type
HUMAN OTC DRUG
Nonproprietary name
Plumbum 8X
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
LEAD
Active strength
8 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-8362-12025-01-30C16284748780-12cef2736-a762-d83d-e063-dadaa90ab31fPlumbum 8X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8362-1Plumbum 8X10 in 1 BOXLIQUID101
48951-8362-1Plumbum 8X1 mL in 1 AMPULELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8362PLUMBUM 8X LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 2 package rows20191210_994b027a-d7d2-7fb1-e053-2a95a90a3f96.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8362-14895183620110 AMPULE in 1 BOX (48951-8362-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent