Vanilla - 36987-1750-4 - (Vanilla)

Alphabetical Index


Drug Information of Vanilla

Product NDC: 36987-1750
Proprietary Name: Vanilla
Non Proprietary Name: Vanilla
Active Ingredient(s): .05    g/mL & nbsp;   Vanilla
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vanilla

Product NDC: 36987-1750
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Vanilla

Package NDC: 36987-1750-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1750-4)

NDC Information of Vanilla

NDC Code 36987-1750-4
Proprietary Name Vanilla
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1750-4)
Product NDC 36987-1750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Vanilla
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name VANILLA
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Food Additives [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Vanilla


General Information