Lentil - 49288-0290-4 - (Lentil)

Alphabetical Index


Drug Information of Lentil

Product NDC: 49288-0290
Proprietary Name: Lentil
Non Proprietary Name: Lentil
Active Ingredient(s): .05    g/mL & nbsp;   Lentil
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lentil

Product NDC: 49288-0290
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Lentil

Package NDC: 49288-0290-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0290-4)

NDC Information of Lentil

NDC Code 49288-0290-4
Proprietary Name Lentil
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0290-4)
Product NDC 49288-0290
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lentil
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name LENTIL
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient]

Complete Information of Lentil


General Information