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CREEPING BENT GRASS POLLEN - 54575-083-30 - (agrostis stolonifera pollen)

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Drug Information of CREEPING BENT GRASS POLLEN

Product NDC: 54575-083
Proprietary Name: CREEPING BENT GRASS POLLEN
Non Proprietary Name: agrostis stolonifera pollen
Active Ingredient(s): 1    g/20mL & nbsp;   agrostis stolonifera pollen
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CREEPING BENT GRASS POLLEN

Product NDC: 54575-083
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of CREEPING BENT GRASS POLLEN

Package NDC: 54575-083-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (54575-083-30)

NDC Information of CREEPING BENT GRASS POLLEN

NDC Code 54575-083-30
Proprietary Name CREEPING BENT GRASS POLLEN
Package Description 30 mL in 1 VIAL, MULTI-DOSE (54575-083-30)
Product NDC 54575-083
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name agrostis stolonifera 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 AGROSTIS STOLONIFERA POLLEN
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE]

Complete Information of CREEPING BENT GRASS POLLEN


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