Paprika - 49288-0376-1 - (Paprika)

Alphabetical Index


Drug Information of Paprika

Product NDC: 49288-0376
Proprietary Name: Paprika
Non Proprietary Name: Paprika
Active Ingredient(s): .05    g/mL & nbsp;   Paprika
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Paprika

Product NDC: 49288-0376
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Paprika

Package NDC: 49288-0376-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0376-1)

NDC Information of Paprika

NDC Code 49288-0376-1
Proprietary Name Paprika
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0376-1)
Product NDC 49288-0376
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paprika
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name PAPRIKA
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],Food Additives [Chemical/Ingredient]

Complete Information of Paprika


General Information