LAMB - 0268-6149-06 - (Lamb)

Alphabetical Index


Drug Information of LAMB

Product NDC: 0268-6149
Proprietary Name: LAMB
Non Proprietary Name: Lamb
Active Ingredient(s): .1    g/mL & nbsp;   Lamb
Administration Route(s): PERCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of LAMB

Product NDC: 0268-6149
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of LAMB

Package NDC: 0268-6149-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6149-06)

NDC Information of LAMB

NDC Code 0268-6149-06
Proprietary Name LAMB
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6149-06)
Product NDC 0268-6149
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Lamb
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name LAMB
Strength Number .1
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],Meat Proteins [Chemical/Ingredient]

Complete Information of LAMB


General Information