FDA.reportPublic FDA data

Anacardium Occidentale

Product NDC
37662-3649
11-digit product format
376623649
Labeler code
37662
Product ID
37662-3649_01e66d3c-0a9b-0871-e063-6394a90ae891
Type
HUMAN OTC DRUG
Nonproprietary name
Anacardium Occidentale
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-08-01
Substance
ANACARDIUM OCCIDENTALE FRUIT
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
Anacardium Occidentale
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANACARDIUM OCCIDENTALE FRUIT12 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4A10JR4E7E

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3649-1Anacardium Occidentale200 in 1 VIAL, GLASSPELLET2001
37662-3649-2Anacardium Occidentale1200 in 1 BOTTLE, GLASSPELLET12001
37662-3649-3Anacardium Occidentale4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3649ANACARDIUM OCCIDENTALE PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 3 package rows20230802_01e66d35-229b-cf1a-e063-6294a90ad034.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3649-137662364901200 PELLET in 1 VIAL, GLASS (37662-3649-1) 200 pellet2023-08-01NoNoCurrent
37662-3649-2376623649021200 PELLET in 1 BOTTLE, GLASS (37662-3649-2) 1200 pellet2023-08-01NoNoCurrent
37662-3649-3376623649034000 PELLET in 1 BOTTLE, GLASS (37662-3649-3) 4000 pellet2023-08-01NoNoCurrent