Apis Levisticum

Product NDC
48951-1058
11-digit product format
489511058
Labeler code
48951
Product ID
48951-1058_69f9b909-330d-aaf0-e053-2a91aa0abc8a
Type
HUMAN OTC DRUG
Nonproprietary name
Apis Levisticum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
APIS MELLIFERA; LEVISTICUM OFFICINALE ROOT
Active strength
3 [hp_X]/mL; [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
48951-1058-1Apis Levisticum10 in 1 BOXLIQUID104
48951-1058-1Apis Levisticum1 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43ZAPIS LEVISTICUM LIQUID [URIEL PHARMACY INC.]1
LEVISTICUM OFFICINALE ROOTACTIVE INGREDIENT46QZ19OEX8APIS LEVISTICUM LIQUID [URIEL PHARMACY INC.]1
APIS MELLIFERAACTIVE MOIETY7S82P3R43ZAPIS LEVISTICUM LIQUID [URIEL PHARMACY INC.]1
LEVISTICUM OFFICINALE ROOTACTIVE MOIETY46QZ19OEX8APIS LEVISTICUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XAPIS LEVISTICUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RAPIS LEVISTICUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1058APIS LEVISTICUM LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20231031_ea5fe924-64d5-4910-9e26-8078aceb5305.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1058-14895110580110 AMPULE in 1 BOX (48951-1058-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent