DROSERA

Product NDC
76472-4079
11-digit product format
764724079
Labeler code
76472
Product ID
76472-4079_2dcc7c60-2737-ff37-e063-6294a90a2410
Type
HUMAN OTC DRUG
Nonproprietary name
DROSERA
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-08
Substance
DROSERA ANGLICA
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
DROSERA
Brand name suffix
200CK
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DROSERA ANGLICA200 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiJ61BY05EGY

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-4079-1DROSERA200CK80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-4079DROSERA 200CK (DROSERA) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250212_ee1323ad-ce95-901e-e053-2995a90aba18.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-4079-17647240790180 PELLET in 1 CYLINDER (76472-4079-1) 80 pellet2022-07-080000-00-00NoNoCurrent