FDA.reportPublic FDA data

Drosera Rotundifolia

Product NDC
37662-0642
11-digit product format
376620642
Labeler code
37662
Product ID
37662-0642_e1e64a61-d0eb-0f8e-e053-2a95a90af186
Type
HUMAN OTC DRUG
Nonproprietary name
Drosera Rotundifolia
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-06-20
Substance
DROSERA ROTUNDIFOLIA WHOLE
Active strength
6 [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 Rotundifolia
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DROSERA ROTUNDIFOLIA WHOLE6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiQR44N9XPJQ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0642-1Drosera Rotundifolia200 in 1 VIAL, GLASSPELLET2001
37662-0642-2Drosera Rotundifolia1200 in 1 BOTTLE, GLASSPELLET12001
37662-0642-3Drosera Rotundifolia4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0642DROSERA ROTUNDIFOLIA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220623_e1e64a61-d0ea-0f8e-e053-2a95a90af186.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0642-137662064201200 PELLET in 1 VIAL, GLASS (37662-0642-1) 200 pellet2022-06-200000-00-00NoNoCurrent
37662-0642-2376620642021200 PELLET in 1 BOTTLE, GLASS (37662-0642-2) 1200 pellet2022-06-200000-00-00NoNoCurrent
37662-0642-3376620642034000 PELLET in 1 BOTTLE, GLASS (37662-0642-3) 4000 pellet2022-06-200000-00-00NoNoCurrent