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POST OAK POLLEN - 54575-955-02 - (quercus stellata pollen)

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Drug Information of POST OAK POLLEN

Product NDC: 54575-955
Proprietary Name: POST OAK POLLEN
Non Proprietary Name: quercus stellata pollen
Active Ingredient(s): 1    g/20mL & nbsp;   quercus stellata pollen
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of POST OAK POLLEN

Product NDC: 54575-955
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of POST OAK POLLEN

Package NDC: 54575-955-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-955-02)

NDC Information of POST OAK POLLEN

NDC Code 54575-955-02
Proprietary Name POST OAK POLLEN
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-955-02)
Product NDC 54575-955
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name quercus stellata 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 STELLATA POLLEN
Strength Number 1
Strength Unit 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]

Complete Information of POST OAK POLLEN


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