Cantharis

Product NDC
76472-3010
11-digit product format
764723010
Labeler code
76472
Product ID
76472-3010_35b722d4-ce27-088e-e063-6394a90a9b8d
Type
HUMAN OTC DRUG
Nonproprietary name
LYTTA VESICATORIA
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-11-22
Substance
LYTTA VESICATORIA
Active strength
200 [kp_C]/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
Brand name suffix
200ck
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LYTTA VESICATORIA200 [kp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3Q034RO3BT

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-3010-1Cantharis200ck80 in 1 CYLINDERPELLET806

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-3010CANTHARIS 200CK (LYTTA VESICATORIA) PELLET [SEVENE USA]6Current NDC, Legacy NDC, 1 package rows20250523_c8d55407-73f9-9c5e-e053-2a95a90a3095.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-3010-17647230100180 PELLET in 1 CYLINDER (76472-3010-1) 80 pellet2011-11-220000-00-00NoNoCurrent