Home NDC 76472-4081-1 EUPHRASIA OFFICINALIS
Product NDC 76472-4081
Requested package NDC 76472-4081-1
11-digit product format 764724081
Labeler code 76472
Product ID 76472-4081_2dcc6b23-698e-358d-e063-6394a90af228
Type HUMAN OTC DRUG
Nonproprietary name EUPHRASIA OFFICINALIS
Dosage form PELLET
Route SUBLINGUAL
Labeler SEVENE USA
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-07-08
Substance EUPHRASIA STRICTA
Active strength 200 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 3 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 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 76472-4081 76472-4081-1 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76472-4081 76472-4081-1 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76472-4081 76472-4081-1 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base EUPHRASIA OFFICINALIS
Brand name suffix 200CK
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength EUPHRASIA STRICTA 200 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C9642I91WL Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76472-4081-1 EUPHRASIA OFFICINALIS200CK 80 in 1 CYLINDER PELLET 80 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76472-4081 EUPHRASIA OFFICINALIS 200CK (EUPHRASIA OFFICINALIS) PELLET [SEVENE USA] 4 Current NDC, Legacy NDC, 1 package rows 20250212_ee12ecae-3a03-5c47-e053-2995a90a8c0d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76472-4081-1 76472408101 80 PELLET in 1 CYLINDER (76472-4081-1) 80 pellet 2022-07-08 0000-00-00 No No Current