Kapok - 49643-017-05 - (Kapok)

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Drug Information of Kapok

Product NDC: 49643-017
Proprietary Name: Kapok
Non Proprietary Name: Kapok
Active Ingredient(s): 1    g/10mL & nbsp;   Kapok
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kapok

Product NDC: 49643-017
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Kapok

Package NDC: 49643-017-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49643-017-05)

NDC Information of Kapok

NDC Code 49643-017-05
Proprietary Name Kapok
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49643-017-05)
Product NDC 49643-017
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Kapok
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name CEIBA PENTANDRA FIBER
Strength Number 1
Strength Unit g/10mL
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 Kapok


General Information