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CEIBA PENTANDRA FIBER - 0268-0635-50 - (KAPOK)

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Drug Information of CEIBA PENTANDRA FIBER

Product NDC: 0268-0635
Proprietary Name: CEIBA PENTANDRA FIBER
Non Proprietary Name: KAPOK
Active Ingredient(s): .05    g/mL & nbsp;   KAPOK
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CEIBA PENTANDRA FIBER

Product NDC: 0268-0635
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of CEIBA PENTANDRA FIBER

Package NDC: 0268-0635-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0635-50)

NDC Information of CEIBA PENTANDRA FIBER

NDC Code 0268-0635-50
Proprietary Name CEIBA PENTANDRA FIBER
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0635-50)
Product NDC 0268-0635
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name KAPOK
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name CEIBA PENTANDRA 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 CEIBA PENTANDRA FIBER


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