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Virginia Live Oak - 36987-2879-3 - (Virginia Live Oak)

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Drug Information of Virginia Live Oak

Product NDC: 36987-2879
Proprietary Name: Virginia Live Oak
Non Proprietary Name: Virginia Live Oak
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Virginia Live Oak
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Virginia Live Oak

Product NDC: 36987-2879
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Virginia Live Oak

Package NDC: 36987-2879-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2879-3)

NDC Information of Virginia Live Oak

NDC Code 36987-2879-3
Proprietary Name Virginia Live Oak
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2879-3)
Product NDC 36987-2879
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Virginia Live 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 VIRGINIANA 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 Virginia Live Oak


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