Viscum Abietis Series 2 7ml

Product NDC
48951-9264
11-digit product format
489519264
Labeler code
48951
Product ID
48951-9264_6bdd135f-b09f-7dcd-e053-2a91aa0a740d
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Abietis Series 2 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
48951-9264-1Viscum Abietis Series 2 7ml7 in 1 BOXLIQUID75
48951-9264-1Viscum Abietis Series 2 7ml1 mL in 1 AMPULELIQUID15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM ABIETIS SERIES 2 7ML LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM ABIETIS SERIES 2 7ML LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XVISCUM ABIETIS SERIES 2 7ML LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RVISCUM ABIETIS SERIES 2 7ML LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9264VISCUM ABIETIS SERIES 2 7ML LIQUID [URIEL PHARMACY INC.]5Legacy NDC, 2 package rows20241207_647e906b-71cb-482b-8f75-a00bf2180fe9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9264-1489519264017 AMPULE in 1 BOX (48951-9264-1) > 1 mL in 1 AMPULE7 ampule2014-08-010000-00-00NoNoCurrent