Sesame - 36987-1739-3 - (Sesame)

Alphabetical Index


Drug Information of Sesame

Product NDC: 36987-1739
Proprietary Name: Sesame
Non Proprietary Name: Sesame
Active Ingredient(s): .05    g/mL & nbsp;   Sesame
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sesame

Product NDC: 36987-1739
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Sesame

Package NDC: 36987-1739-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1739-3)

NDC Information of Sesame

NDC Code 36987-1739-3
Proprietary Name Sesame
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1739-3)
Product NDC 36987-1739
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sesame
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name SESAME SEED
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],Seed Storage Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient]

Complete Information of Sesame


General Information