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California Valley White Oak - 36987-2871-1 - (California Valley White Oak)

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Drug Information of California Valley White Oak

Product NDC: 36987-2871
Proprietary Name: California Valley White Oak
Non Proprietary Name: California Valley White Oak
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   California Valley White Oak
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of California Valley White Oak

Product NDC: 36987-2871
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of California Valley White Oak

Package NDC: 36987-2871-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-2871-1)

NDC Information of California Valley White Oak

NDC Code 36987-2871-1
Proprietary Name California Valley White Oak
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-2871-1)
Product NDC 36987-2871
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name California Valley White 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 LOBATA 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 California Valley White Oak


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