Kapok - 36987-2229-1 - (Kapok)

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Drug Information of Kapok

Product NDC: 36987-2229
Proprietary Name: Kapok
Non Proprietary Name: Kapok
Active Ingredient(s): .1    g/mL & nbsp;   Kapok
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kapok

Product NDC: 36987-2229
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Kapok

Package NDC: 36987-2229-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-2229-1)

NDC Information of Kapok

NDC Code 36987-2229-1
Proprietary Name Kapok
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-2229-1)
Product NDC 36987-2229
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Kapok
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name CEIBA PENTANDRA 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 Kapok


General Information