22840-1003 NDC - FIRE ANT (SOLENOPSIS INVICTA)

Drug Information

Product NDC: 22840-1003

Proprietary Name: Fire Ant

Non Proprietary Name: Solenopsis invicta

Active Ingredient(s):
  • .001 g/mL SOLENOPSIS INVICTA


Administration Route(s): INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS

Dosage Form(s): SOLUTION

Pharmacy Class(es):
  • Non-Standardized Insect Venom Allergenic Extract [EPC];
  • Increased Histamine Release [PE];
  • Cell-mediated Immunity [PE];
  • Increased IgG Production [PE];
  • Insect Proteins [CS];
  • Ant Venoms [CS];
  • Allergens [CS]

Labeler Information

Labeler Name: Greer Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA101833
Marketing Category: BLA
Start Marketing Date:9/15/1981

Package Information

No. Package Code Package Description Billing Unit
122840-1003-15 mL in 1 VIAL, MULTI-DOSE (22840-1003-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC22840-1003The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMENON-STANDARDIZED ALLERGENICIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEFire AntThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMESolenopsis invictaThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEINTRADERMAL; PERCUTANEOUS; SUBCUTANEOUSThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/15/1981This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEBLAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERBLA101833This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEGreer Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMESOLENOPSIS INVICTAThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.001 
ACTIVE INGRED UNITg/mL 
PHARM CLASSESNon-Standardized Insect Venom Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Insect Proteins [CS],Ant Venoms [CS],Allergens [CS] 

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This page was last updated on: 8/16/2019