FDA.reportPublic FDA data

Anagallis Arvensis

Product NDC
37662-3666
11-digit product format
376623666
Labeler code
37662
Product ID
37662-3666_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
30 [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 WHOLE30 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii46883LR90E

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3666-1Anagallis Arvensis80 in 1 VIAL, GLASSPELLET801
37662-3666-2Anagallis Arvensis200 in 1 VIAL, GLASSPELLET2001
37662-3666-3Anagallis Arvensis1200 in 1 BOTTLE, GLASSPELLET12001
37662-3666-4Anagallis Arvensis4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3666ANAGALLIS ARVENSIS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230803_01fa040d-3803-f311-e063-6294a90ab18a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3666-13766236660180 PELLET in 1 VIAL, GLASS (37662-3666-1) 80 pellet2023-08-02NoNoCurrent
37662-3666-237662366602200 PELLET in 1 VIAL, GLASS (37662-3666-2) 200 pellet2023-08-02NoNoCurrent
37662-3666-3376623666031200 PELLET in 1 BOTTLE, GLASS (37662-3666-3) 1200 pellet2023-08-02NoNoCurrent
37662-3666-4376623666044000 PELLET in 1 BOTTLE, GLASS (37662-3666-4) 4000 pellet2023-08-02NoNoCurrent