FDA.reportPublic FDA data

ACONITE NAPELLIS

Product NDC
54973-2900
Requested package NDC
54973-2900-4
11-digit product format
549732900
Labeler code
54973
Product ID
54973-2900_9c0c23a8-ff17-f150-e053-2a95a90ace56
Type
HUMAN OTC DRUG
Nonproprietary name
aconitum napellus root
Dosage form
TABLET
Route
ORAL
Labeler
Hyland's
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1955-01-01
Marketing end
0000-00-00
Substance
ACONITUM NAPELLUS ROOT
Active strength
30 [hp_X]/1
NDC exclude flag
No
Listing certified through
2021-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage54973-290054973-2900-4DDiscontinued by firm2026-07-31

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM NAPELLUS ROOTACTIVE INGREDIENTKPD2N7348XACONITE NAPELLIS (ACONITUM NAPELLUS ROOT) TABLET [HYLAND'S]1
ACONITUM NAPELLUS ROOTACTIVE MOIETYKPD2N7348XACONITE NAPELLIS (ACONITUM NAPELLUS ROOT) TABLET [HYLAND'S]1
ACACIAINACTIVE INGREDIENT5C5403N26OACONITE NAPELLIS (ACONITUM NAPELLUS ROOT) TABLET [HYLAND'S]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GACONITE NAPELLIS (ACONITUM NAPELLUS ROOT) TABLET [HYLAND'S]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
54973-2900-454973290004250 TABLET in 1 BOTTLE, PLASTIC (54973-2900-4) 250 tablet1955-01-010000-00-00NoNoCurrent