Home > National Drug Code (NDC) > Giant Wild Rye

Giant Wild Rye - 36987-2378-3 - (Giant Wild Rye)

Alphabetical Index


Drug Information of Giant Wild Rye

Product NDC: 36987-2378
Proprietary Name: Giant Wild Rye
Non Proprietary Name: Giant Wild Rye
Active Ingredient(s): .05    g/mL & nbsp;   Giant Wild Rye
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Giant Wild Rye

Product NDC: 36987-2378
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Giant Wild Rye

Package NDC: 36987-2378-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2378-3)

NDC Information of Giant Wild Rye

NDC Code 36987-2378-3
Proprietary Name Giant Wild Rye
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2378-3)
Product NDC 36987-2378
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Giant Wild Rye
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name LEYMUS CONDENSATUS POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Giant Wild Rye


General Information