Jute - 36987-2252-2 - (Jute)

Alphabetical Index


Drug Information of Jute

Product NDC: 36987-2252
Proprietary Name: Jute
Non Proprietary Name: Jute
Active Ingredient(s): .1    g/mL & nbsp;   Jute
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Jute

Product NDC: 36987-2252
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Jute

Package NDC: 36987-2252-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-2252-2)

NDC Information of Jute

NDC Code 36987-2252-2
Proprietary Name Jute
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-2252-2)
Product NDC 36987-2252
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Jute
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name CORCORUS CAPSULARIS FIBER
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Fiber Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Plant Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Jute


General Information