Cantaloupe - 49288-0102-2 - (Cantaloupe)

Alphabetical Index


Drug Information of Cantaloupe

Product NDC: 49288-0102
Proprietary Name: Cantaloupe
Non Proprietary Name: Cantaloupe
Active Ingredient(s): .05    g/mL & nbsp;   Cantaloupe
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cantaloupe

Product NDC: 49288-0102
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Cantaloupe

Package NDC: 49288-0102-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0102-2)

NDC Information of Cantaloupe

NDC Code 49288-0102-2
Proprietary Name Cantaloupe
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0102-2)
Product NDC 49288-0102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cantaloupe
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name CANTALOUPE
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Fruit Proteins [Chemical/Ingredient]

Complete Information of Cantaloupe


General Information