FDA.reportPublic FDA data

Plumbum met. 20 Special Order

Product NDC
48951-8341
11-digit product format
489518341
Labeler code
48951
Product ID
48951-8341_6d0aa18c-56ca-1e07-e053-2a91aa0aac92
Type
HUMAN OTC DRUG
Nonproprietary name
Plumbum met. 20 Special Order
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
20 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-8341IInactivated by FDA2026-08-10
excluded packagepackage48951-834148951-8341-1IInactivated by FDA2026-08-10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8341-1Plumbum met. 20 Special Order10 in 1 BOXLIQUID101
48951-8341-1Plumbum met. 20 Special Order1 mL in 1 AMPULELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8341PLUMBUM MET. 20 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 2 package rows20180525_6d0aa18c-56c9-1e07-e053-2a91aa0aac92.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8341-14895183410110 AMPULE in 1 BOX (48951-8341-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent