Apple - 49288-0010-4 - (Apple)

Alphabetical Index


Drug Information of Apple

Product NDC: 49288-0010
Proprietary Name: Apple
Non Proprietary Name: Apple
Active Ingredient(s): .05    g/mL & nbsp;   Apple
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Apple

Product NDC: 49288-0010
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Apple

Package NDC: 49288-0010-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0010-4)

NDC Information of Apple

NDC Code 49288-0010-4
Proprietary Name Apple
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0010-4)
Product NDC 49288-0010
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Apple
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name APPLE
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Fruit Proteins [Chemical/Ingredient],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE]

Complete Information of Apple


General Information