Anacardium

Product NDC
53645-1491
11-digit product format
536451491
Labeler code
53645
Product ID
53645-1491_f031aed9-884d-e9b9-e053-2a95a90aace1
Type
HUMAN OTC DRUG
Nonproprietary name
Anacardium
Dosage form
LIQUID
Route
ORAL
Labeler
True Botanica, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-02-03
Marketing end
0000-00-00
Substance
ANACARDIUM OCCIDENTALE FRUIT
Active strength
30 [hp_X]/55mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53645-1491-32024-01-30C16284748780-11030e365-4f31-111a-e063-dadaa90a10e2Anacardium Orientale 30X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53645-1491-3Anacardium55 mL in 1 BOTTLELIQUID553

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53645-1491ANACARDIUM LIQUID [TRUE BOTANICA, LLC]3Legacy NDC, 1 package rows20221220_9c8af81a-8925-5c3d-e053-2a95a90a136f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53645-1491-35364514910355 mL in 1 BOTTLE (53645-1491-3) 55 ml2014-02-030000-00-00NoNoCurrent