Viscum Abietis Series 3 7ml

Product NDC
48951-9265
11-digit product format
489519265
Labeler code
48951
Product ID
48951-9265_6bdd435f-03e3-236d-e053-2991aa0a2306
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Abietis Series 3 7ml
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
VISCUM ALBUM FRUITING TOP
Active strength
1 [hp_X]/mL
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
48951-9265-1Viscum Abietis Series 3 7ml1 mL in 1 AMPULELIQUID15
48951-9265-1Viscum Abietis Series 3 7ml7 in 1 BOXLIQUID75

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM ABIETIS SERIES 3 7ML LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM ABIETIS SERIES 3 7ML LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XVISCUM ABIETIS SERIES 3 7ML LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RVISCUM ABIETIS SERIES 3 7ML LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9265VISCUM ABIETIS SERIES 3 7ML LIQUID [URIEL PHARMACY INC.]5Legacy NDC, 2 package rows20241207_cb7f53f6-7d7f-4875-bde4-a4d69f840965.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9265-1489519265017 AMPULE in 1 BOX (48951-9265-1) > 1 mL in 1 AMPULE7 ampule2014-08-010000-00-00NoNoCurrent