EUPHRASIA OFFICINALIS

Product NDC
76472-4081
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

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
IngredientStrength
EUPHRASIA STRICTA200 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiC9642I91WL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-4081-1EUPHRASIA OFFICINALIS200CK80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-4081EUPHRASIA OFFICINALIS 200CK (EUPHRASIA OFFICINALIS) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250212_ee12ecae-3a03-5c47-e053-2995a90a8c0d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-4081-17647240810180 PELLET in 1 CYLINDER (76472-4081-1) 80 pellet2022-07-080000-00-00NoNoCurrent