FDA.reportPublic FDA data

Aconitum

Product NDC
53645-1610
11-digit product format
536451610
Labeler code
53645
Product ID
53645-1610_f0312815-fc62-1ff3-e053-2995a90ac4c4
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum
Dosage form
GLOBULE
Route
ORAL
Labeler
True Botanica, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-11-24
Marketing end
0000-00-00
Substance
ACONITUM NAPELLUS ROOT
Active strength
30 [hp_X]/23g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct53645-1610DDiscontinued by firm2026-07-31
excluded packagepackage53645-161053645-1610-2DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53645-1610-22021-01-31C16284748780-1ba0f9c33-49c5-a910-e053-dadaa90a0b85Aconitum 30x
53645-1610-22021-01-29C16284748780-1ba0f9c33-49c5-a910-e053-dadaa90a0b85Aconitum 30x

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53645-1610ACONITUM GLOBULE [TRUE BOTANICA, LLC]5Legacy NDC20230502_61870547-8bb3-35ff-e053-2a91aa0a2a50.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53645-1610-25364516100223 g in 1 BOTTLE (53645-1610-2) 23 g2017-11-240000-00-00NoNoCurrent