Rhus Glabra

Product NDC
37662-1379
11-digit product format
376621379
Labeler code
37662
Product ID
37662-1379_e68d0227-13a9-c6be-e053-2a95a90aacbd
Type
HUMAN OTC DRUG
Nonproprietary name
Rhus Glabra
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-08-18
Substance
RHUS GLABRA TOP
Active strength
1 [hp_Q]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Rhus Glabra
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
RHUS GLABRA TOP1 [hp_Q]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiRHH784E0K6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-1379-1Rhus Glabra10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-1379RHUS GLABRA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 1 package rows20220820_e68d0227-13a8-c6be-e053-2a95a90aacbd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-1379-13766213790110000 PELLET in 1 BOTTLE, GLASS (37662-1379-1) 10000 pellet2022-08-180000-00-00NoNoCurrent