Cantharis

Product NDC
0220-1145
11-digit product format
002201145
Labeler code
0220
Product ID
0220-1145_09bed294-41b6-4800-e063-6394a90afef4
Type
HUMAN OTC DRUG
Nonproprietary name
LYTTA VESICATORIA
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
LYTTA VESICATORIA
Active strength
30 [hp_X]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cantharis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LYTTA VESICATORIA30 [hp_X]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3Q034RO3BT

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-1145-412023-11-09C16284748780-1f386c649-d600-0266-e053-dadaa90a7c1aCantharis 30X
0220-1145-412023-01-30C16284748780-1f386c649-d600-0266-e053-dadaa90a7c1aCantharis 30X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-1145-41Cantharis80 in 1 TUBEPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-1145CANTHARIS (LYTTA VESICATORIA) PELLET [BOIRON]4Current NDC, Legacy NDC, 1 package rows20231110_6f3a6130-7a53-11e6-b587-424c58303031.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0220-1145-410022011454180 PELLET in 1 TUBE (0220-1145-41) 80 pellet1983-03-030000-00-00NoNoCurrent