Plum - 49288-0406-2 - (Plum)

Alphabetical Index


Drug Information of Plum

Product NDC: 49288-0406
Proprietary Name: Plum
Non Proprietary Name: Plum
Active Ingredient(s): 1    mL/mL & nbsp;   Plum
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Plum

Product NDC: 49288-0406
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Plum

Package NDC: 49288-0406-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0406-2)

NDC Information of Plum

NDC Code 49288-0406-2
Proprietary Name Plum
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0406-2)
Product NDC 49288-0406
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Plum
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name PLUM
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 Plum


General Information