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California Black Oak - 36987-2839-3 - (California Black Oak)

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Drug Information of California Black Oak

Product NDC: 36987-2839
Proprietary Name: California Black Oak
Non Proprietary Name: California Black Oak
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   California Black Oak
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of California Black Oak

Product NDC: 36987-2839
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 Black Oak

Package NDC: 36987-2839-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2839-3)

NDC Information of California Black Oak

NDC Code 36987-2839-3
Proprietary Name California Black Oak
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2839-3)
Product NDC 36987-2839
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name California Black 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 KELLOGGII 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 Black Oak


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