Coconut - 36987-1539-3 - (Coconut)

Alphabetical Index


Drug Information of Coconut

Product NDC: 36987-1539
Proprietary Name: Coconut
Non Proprietary Name: Coconut
Active Ingredient(s): .05    g/mL & nbsp;   Coconut
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Coconut

Product NDC: 36987-1539
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Coconut

Package NDC: 36987-1539-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1539-3)

NDC Information of Coconut

NDC Code 36987-1539-3
Proprietary Name Coconut
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1539-3)
Product NDC 36987-1539
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Coconut
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name COCONUT
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],Fruit Proteins [Chemical/Ingredient]

Complete Information of Coconut


General Information