Home NDC 48951-9171 Aconitum e tub. 30
Product NDC 48951-9171
11-digit product format 489519171
Labeler code 48951
Product ID 48951-9171_c68ebe6c-88a0-12ee-e053-2a95a90a97e4
Type HUMAN OTC DRUG
Nonproprietary name Aconitum e tub. 30
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Marketing end 0000-00-00
Substance ACONITUM NAPELLUS
Active strength 30 [hp_X]/mL
NDC exclude flag No
Listing certified through 2022-12-31
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 · 2 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product 48951-9171 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 48951-9171 48951-9171-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-9171 ACONITUM E TUB. 30 LIQUID [URIEL PHARMACY INC.] 6 Legacy NDC 20210708_8b80552a-6ae3-40ea-bf41-5cd705be04f2.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-9171-1 48951917101 10 AMPULE in 1 BOX (48951-9171-1) > 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current