Lobster - 49288-0291-1 - (Lobster)

Alphabetical Index


Drug Information of Lobster

Product NDC: 49288-0291
Proprietary Name: Lobster
Non Proprietary Name: Lobster
Active Ingredient(s): .05    g/mL & nbsp;   Lobster
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lobster

Product NDC: 49288-0291
Labeler Name: Antigen Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Lobster

Package NDC: 49288-0291-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0291-1)

NDC Information of Lobster

NDC Code 49288-0291-1
Proprietary Name Lobster
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0291-1)
Product NDC 49288-0291
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Lobster
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name LOBSTER
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 Lobster


General Information