RUTA GRAVEOLENS

Product NDC
76472-3032
11-digit product format
764723032
Labeler code
76472
Product ID
76472-3032_2dcc6b2e-b3d5-e17b-e063-6294a90a2fd2
Type
HUMAN OTC DRUG
Nonproprietary name
RUTA GRAVEOLENS
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-11-23
Substance
RUTA GRAVEOLENS FLOWERING TOP
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
RUTA GRAVEOLENS
Brand name suffix
200ck
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
RUTA GRAVEOLENS FLOWERING TOP200 [kp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiN94C2U587S

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-3032-1RUTA GRAVEOLENS200ck80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-3032RUTA GRAVEOLENS 200CK (RUTA GRAVEOLENS) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250212_cf898a11-a78e-342d-e053-2995a90a5b05.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-3032-17647230320180 PELLET in 1 CYLINDER (76472-3032-1) 80 pellet2011-11-230000-00-00NoNoCurrent