Cashew - 36987-1535-4 - (Cashew)

Alphabetical Index


Drug Information of Cashew

Product NDC: 36987-1535
Proprietary Name: Cashew
Non Proprietary Name: Cashew
Active Ingredient(s): .05    g/mL & nbsp;   Cashew
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cashew

Product NDC: 36987-1535
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Cashew

Package NDC: 36987-1535-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1535-4)

NDC Information of Cashew

NDC Code 36987-1535-4
Proprietary Name Cashew
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1535-4)
Product NDC 36987-1535
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cashew
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name CASHEW
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Nut Proteins [Chemical/Ingredient]

Complete Information of Cashew


General Information