Burrobrush - 36987-3153-4 - (Burrobrush)

Alphabetical Index


Drug Information of Burrobrush

Product NDC: 36987-3153
Proprietary Name: Burrobrush
Non Proprietary Name: Burrobrush
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Burrobrush
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Burrobrush

Product NDC: 36987-3153
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Burrobrush

Package NDC: 36987-3153-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-3153-4)

NDC Information of Burrobrush

NDC Code 36987-3153-4
Proprietary Name Burrobrush
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-3153-4)
Product NDC 36987-3153
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Burrobrush
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name HYMENOCLEA SALSOLA POLLEN
Strength Number 40000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Burrobrush


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