Water Oak - 36987-2887-3 - (Water Oak)

Alphabetical Index


Drug Information of Water Oak

Product NDC: 36987-2887
Proprietary Name: Water Oak
Non Proprietary Name: Water Oak
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Water Oak
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Water Oak

Product NDC: 36987-2887
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Water Oak

Package NDC: 36987-2887-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2887-3)

NDC Information of Water Oak

NDC Code 36987-2887-3
Proprietary Name Water Oak
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2887-3)
Product NDC 36987-2887
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Water Oak
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name QUERCUS NIGRA POLLEN
Strength Number 20000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Water Oak


General Information