FDA.reportPublic FDA data

ACONITE

Product NDC
0360-0004
11-digit product format
003600004
Labeler code
0360
Product ID
0360-0004_7d9f1d26-1b02-0a20-e053-2991aa0a25df
Type
HUMAN OTC DRUG
Nonproprietary name
ACONITE NAPELLUS
Dosage form
TABLET
Route
SUBLINGUAL
Labeler
STANDARD HOMEOPATHIC COMPANY
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1997-02-17
Marketing end
0000-00-00
Substance
ACONITUM NAPELLUS
Active strength
30 [hp_X]/g
NDC exclude flag
No
Listing certified through
2020-12-31
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 productproduct0360-0004DDiscontinued by firm2026-07-31
excluded packagepackage0360-00040360-0004-02DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0360-0004-02003600004021 g in 1 BOTTLE, PLASTIC (0360-0004-02) 1 g1997-02-170000-00-00NoNoCurrent