FDA.reportPublic FDA data

Anagallis Arvensis

Product NDC
37662-3665
11-digit product format
376623665
Labeler code
37662
Product ID
37662-3665_01fa3e6c-b834-73c0-e063-6394a90ad949
Type
HUMAN OTC DRUG
Nonproprietary name
Anagallis Arvensis
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-08-02
Substance
ANAGALLIS ARVENSIS WHOLE
Active strength
12 [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
Anagallis Arvensis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANAGALLIS ARVENSIS WHOLE12 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii46883LR90E

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3665-1Anagallis Arvensis200 in 1 VIAL, GLASSPELLET2001
37662-3665-2Anagallis Arvensis1200 in 1 BOTTLE, GLASSPELLET12001
37662-3665-3Anagallis Arvensis4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3665ANAGALLIS ARVENSIS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 3 package rows20230803_01fa040d-3803-f311-e063-6294a90ab18a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3665-137662366501200 PELLET in 1 VIAL, GLASS (37662-3665-1) 200 pellet2023-08-02NoNoCurrent
37662-3665-2376623665021200 PELLET in 1 BOTTLE, GLASS (37662-3665-2) 1200 pellet2023-08-02NoNoCurrent
37662-3665-3376623665034000 PELLET in 1 BOTTLE, GLASS (37662-3665-3) 4000 pellet2023-08-02NoNoCurrent