Home > National Drug Code (NDC) > COTTON FIBER

COTTON FIBER - 0268-0609-10 - (COTTON LINTERS)

Alphabetical Index


Drug Information of COTTON FIBER

Product NDC: 0268-0609
Proprietary Name: COTTON FIBER
Non Proprietary Name: COTTON LINTERS
Active Ingredient(s): .05    g/mL & nbsp;   COTTON LINTERS
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of COTTON FIBER

Product NDC: 0268-0609
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of COTTON FIBER

Package NDC: 0268-0609-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0609-10)

NDC Information of COTTON FIBER

NDC Code 0268-0609-10
Proprietary Name COTTON FIBER
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0609-10)
Product NDC 0268-0609
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name COTTON LINTERS
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name COTTON FIBER
Strength Number .05
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 COTTON FIBER


General Information