Home NDC 48951-8357-3 Stannum 12X
Product NDC 48951-8357
Requested package NDC 48951-8357-3
11-digit product format 489518357
Labeler code 48951
Product ID 48951-8357_945516af-a064-0975-e053-2995a90a4d1c
Type HUMAN OTC DRUG
Nonproprietary name Stannum 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 TIN
Active strength 12 [hp_X]/mL
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 48951-8357 48951-8357-3 D Discontinued by firm excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-8357-3 Stannum 12X 60 mL in 1 BOTTLE, DROPPER LIQUID 60 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8357 STANNUM 12X LIQUID [URIEL PHARMACY INC.] 3 Legacy NDC, 1 package rows 20240926_945516af-a063-0975-e053-2995a90a4d1c.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-8357-3 48951835703 60 mL in 1 BOTTLE, DROPPER (48951-8357-3) 60 ml 2009-09-01 0000-00-00 No No Current