COCCULUS INDICUS

Product NDC
76472-4076
11-digit product format
764724076
Labeler code
76472
Product ID
76472-4076_2ddc3aac-ab41-ef41-e063-6394a90a04d6
Type
HUMAN OTC DRUG
Nonproprietary name
COCCULUS INDICUS
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-08
Substance
ANAMIRTA COCCULUS SEED
Active strength
200 [hp_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
COCCULUS INDICUS
Brand name suffix
200CK
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANAMIRTA COCCULUS SEED200 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii810258W28U

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-4076-1COCCULUS INDICUS200CK80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-4076COCCULUS INDICUS 200CK (COCCULUS INDICUS) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250213_ed9c7d19-3186-beb8-e053-2995a90a7481.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-4076-17647240760180 PELLET in 1 CYLINDER (76472-4076-1) 80 pellet2022-07-080000-00-00NoNoCurrent