Raspberry - 49288-0439-3 - (Raspberry)

Alphabetical Index


Drug Information of Raspberry

Product NDC: 49288-0439
Proprietary Name: Raspberry
Non Proprietary Name: Raspberry
Active Ingredient(s): 1    mL/mL & nbsp;   Raspberry
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Raspberry

Product NDC: 49288-0439
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Raspberry

Package NDC: 49288-0439-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0439-3)

NDC Information of Raspberry

NDC Code 49288-0439-3
Proprietary Name Raspberry
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0439-3)
Product NDC 49288-0439
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Raspberry
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name RASPBERRY
Strength Number 1
Strength Unit mL/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 Raspberry


General Information