Jute - 36987-2246-4 - (Jute)

Alphabetical Index


Drug Information of Jute

Product NDC: 36987-2246
Proprietary Name: Jute
Non Proprietary Name: Jute
Active Ingredient(s): 10000    [PNU]/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: 36987-2246
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: 36987-2246-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-2246-4)

NDC Information of Jute

NDC Code 36987-2246-4
Proprietary Name Jute
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-2246-4)
Product NDC 36987-2246
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 10000
Strength Unit [PNU]/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