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2-OAK MIX, RED/WHITE POLLEN - 54575-952-02 - (quercus rubra pollen and quercus alba pollen)

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Drug Information of 2-OAK MIX, RED/WHITE POLLEN

Product NDC: 54575-952
Proprietary Name: 2-OAK MIX, RED/WHITE POLLEN
Non Proprietary Name: quercus rubra pollen and quercus alba pollen
Active Ingredient(s): .5; .5    g/20mL; g/20mL & nbsp;   quercus rubra pollen and quercus alba pollen
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of 2-OAK MIX, RED/WHITE POLLEN

Product NDC: 54575-952
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of 2-OAK MIX, RED/WHITE POLLEN

Package NDC: 54575-952-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-952-02)

NDC Information of 2-OAK MIX, RED/WHITE POLLEN

NDC Code 54575-952-02
Proprietary Name 2-OAK MIX, RED/WHITE POLLEN
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-952-02)
Product NDC 54575-952
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name quercus rubra pollen and quercus alba pollen
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name QUERCUS ALBA POLLEN; QUERCUS RUBRA POLLEN
Strength Number .5; .5
Strength Unit g/20mL; g/20mL
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],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 2-OAK MIX, RED/WHITE POLLEN


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