FDA.reportPublic FDA data

Lycopodium

Product NDC
44911-0346
Requested package NDC
44911-0346-1
11-digit product format
449110346
Labeler code
44911
Product ID
44911-0346_e41d4612-7969-4fcd-aee2-5c5a8b24601e
Type
HUMAN OTC DRUG
Nonproprietary name
Lycopodium Clavatum
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2016-04-12
Marketing end
2026-04-13
Substance
LYCOPODIUM CLAVATUM SPORE
Active strength
200 [hp_C]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
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 packagepackage44911-034644911-0346-1DDiscontinued by firm2026-07-31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0346LYCOPODIUM (LYCOPODIUM CLAVATUM) LIQUID [ENERGIQUE, INC.]3Legacy NDC20220701_8f407918-aaa0-4609-913e-5058ef79986d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0346-14491103460130 mL in 1 BOTTLE, DROPPER (44911-0346-1) 30 ml2016-04-122026-04-13NoNoCurrent