Helleborus e pl. tota 3 Special Order

Product NDC
48951-5077
11-digit product format
489515077
Labeler code
48951
Product ID
48951-5077_6dd644fb-2a13-044e-e053-2a91aa0a5fb6
Type
HUMAN OTC DRUG
Nonproprietary name
Helleborus e pl. tota 3 Special Order
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
HELLEBORUS FOETIDUS 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
48951-5077-2Helleborus e pl. tota 3 Special Order1350 in 1 BOTTLE, GLASSPELLET13502

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HELLEBORUS FOETIDUS ROOTACTIVE INGREDIENT332Y7EES96HELLEBORUS E PL. TOTA 3 SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
HELLEBORUS FOETIDUS ROOTACTIVE MOIETY332Y7EES96HELLEBORUS E PL. TOTA 3 SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554HELLEBORUS E PL. TOTA 3 SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-5077HELLEBORUS E PL. TOTA 3 SPECIAL ORDER PELLET [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20180605_7aa3e1fe-7c75-4ae0-9272-3d04cb22d97b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-5077-2489515077021350 PELLET in 1 BOTTLE, GLASS (48951-5077-2) 1350 pellet2009-09-010000-00-00NoNoCurrent