FDA.reportPublic FDA data

Anacardium Orientale

Product NDC
37662-3659
11-digit product format
376623659
Labeler code
37662
Product ID
37662-3659_01e691d3-858d-f907-e063-6294a90a5d38
Type
HUMAN OTC DRUG
Nonproprietary name
Anacardium Orientale
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-08-01
Substance
SEMECARPUS ANACARDIUM JUICE
Active strength
100 [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 Orientale
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SEMECARPUS ANACARDIUM JUICE100 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiY0F0BU8RDU

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3659-1Anacardium Orientale200 in 1 VIAL, GLASSPELLET2001
37662-3659-2Anacardium Orientale500 in 1 VIAL, GLASSPELLET5001
37662-3659-3Anacardium Orientale3000 in 1 BOTTLE, GLASSPELLET30001
37662-3659-4Anacardium Orientale10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3659ANACARDIUM ORIENTALE PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230802_01e691d3-858c-f907-e063-6294a90a5d38.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3659-137662365901200 PELLET in 1 VIAL, GLASS (37662-3659-1) 200 pellet2023-08-01NoNoCurrent
37662-3659-237662365902500 PELLET in 1 VIAL, GLASS (37662-3659-2) 500 pellet2023-08-01NoNoCurrent
37662-3659-3376623659033000 PELLET in 1 BOTTLE, GLASS (37662-3659-3) 3000 pellet2023-08-01NoNoCurrent
37662-3659-43766236590410000 PELLET in 1 BOTTLE, GLASS (37662-3659-4) 10000 pellet2023-08-01NoNoCurrent