Apis Belladonna

Product NDC
48951-1045
11-digit product format
489511045
Labeler code
48951
Product ID
48951-1045_48885820-b172-818e-e063-6394a90a7282
Type
HUMAN OTC DRUG
Nonproprietary name
Apis Belladonna
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
APIS MELLIFERA; ATROPA BELLADONNA
Active strength
5; 4 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Apis Belladonna
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ATROPA BELLADONNA5 [hp_X]/mL
APIS MELLIFERA4 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
WQZ3G9PF0HInternal UNII lookup
7S82P3R43ZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8db74171-1580-4459-a3d2-5862ef6aa827Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1045-1Apis Belladonna10 in 1 BOXLIQUID105
48951-1045-1Apis Belladonna1 mL in 1 AMPULELIQUID15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43ZAPIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0HAPIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
APIS MELLIFERAACTIVE MOIETY7S82P3R43ZAPIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0HAPIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XAPIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RAPIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1045APIS BELLADONNA LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20250129_8db74171-1580-4459-a3d2-5862ef6aa827.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Apis BelladonnaAPIS BELLADONNAUriel Pharmacy Inc.8db74171-1580-4459-a3d2-5862ef6aa8272026-01-16WarningsExact identifier
ndc (product): 48951-1045

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1045-14895110450110 AMPULE in 1 BOX (48951-1045-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent