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Grama grass Pollen - 49643-326-05 - (Bouteloua spp.)

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Drug Information of Grama grass Pollen

Product NDC: 49643-326
Proprietary Name: Grama grass Pollen
Non Proprietary Name: Bouteloua spp.
Active Ingredient(s): 1    g/20mL & nbsp;   Bouteloua spp.
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Grama grass Pollen

Product NDC: 49643-326
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Grama grass Pollen

Package NDC: 49643-326-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49643-326-05)

NDC Information of Grama grass Pollen

NDC Code 49643-326-05
Proprietary Name Grama grass Pollen
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49643-326-05)
Product NDC 49643-326
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Bouteloua spp.
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name BOUTELOUA GRACILIS 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 Grama grass Pollen


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