Formica Apis

Product NDC
48951-4193
11-digit product format
489514193
Labeler code
48951
Product ID
48951-4193_45779954-6d64-47f6-e063-6394a90a4293
Type
HUMAN OTC DRUG
Nonproprietary name
Formica Apis
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
APIS MELLIFERA; FORMICA RUFA
Active strength
3; 3 [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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Formica Apis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
APIS MELLIFERA3 [hp_X]/mL
FORMICA RUFA3 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7S82P3R43Z, 55H0W83JO5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4193-1Formica Apis1 mL in 1 AMPULELIQUID12
48951-4193-1Formica Apis10 in 1 BOXLIQUID102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4193FORMICA APIS LIQUID [URIEL PHARMACY INC.]1Current NDC, 2 package rows20241206_285fbafd-f390-49df-e063-6394a90a42c9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-4193-14895141930110 AMPULE in 1 BOX (48951-4193-1) / 1 mL in 1 AMPULE10 ampule2009-09-01NoNoHistorical