Levisticum e rad. 3

Product NDC
48951-6029
11-digit product format
489516029
Labeler code
48951
Product ID
48951-6029_6de61cd6-cdf1-467f-e053-2991aa0a183d
Type
HUMAN OTC DRUG
Nonproprietary name
Levisticum e rad. 3
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
LEVISTICUM OFFICINALE ROOT
Active strength
3 [hp_X]/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-6029-2Levisticum e rad. 31350 in 1 BOTTLE, GLASSPELLET13504

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LEVISTICUM OFFICINALE ROOTACTIVE INGREDIENT46QZ19OEX8LEVISTICUM E RAD. 3 PELLET [URIEL PHARMACY INC.]1
LEVISTICUM OFFICINALE ROOTACTIVE MOIETY46QZ19OEX8LEVISTICUM E RAD. 3 PELLET [URIEL PHARMACY INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554LEVISTICUM E RAD. 3 PELLET [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-6029LEVISTICUM E RAD. 3 PELLET [URIEL PHARMACY INC.]4Legacy NDC, 1 package rows20240112_0f96ce12-a4dd-4043-8f6e-3ad33c3d9c79.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-6029-2489516029021350 PELLET in 1 BOTTLE, GLASS (48951-6029-2) 1350 pellet2009-09-010000-00-00NoNoCurrent