Oyster - 49288-0336-2 - (Oyster)

Alphabetical Index


Drug Information of Oyster

Product NDC: 49288-0336
Proprietary Name: Oyster
Non Proprietary Name: Oyster
Active Ingredient(s): .05    g/mL & nbsp;   Oyster
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Oyster

Product NDC: 49288-0336
Labeler Name: Antigen Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Oyster

Package NDC: 49288-0336-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0336-2)

NDC Information of Oyster

NDC Code 49288-0336-2
Proprietary Name Oyster
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0336-2)
Product NDC 49288-0336
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Oyster
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name OYSTER
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],Shellfish Proteins [Chemical/Ingredient]

Complete Information of Oyster


General Information