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Utah Juniper Pollen - 49643-370-30 - (Juniperus osteosperma)

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Drug Information of Utah Juniper Pollen

Product NDC: 49643-370
Proprietary Name: Utah Juniper Pollen
Non Proprietary Name: Juniperus osteosperma
Active Ingredient(s): 1    g/20mL & nbsp;   Juniperus osteosperma
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Utah Juniper Pollen

Product NDC: 49643-370
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Utah Juniper Pollen

Package NDC: 49643-370-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49643-370-30)

NDC Information of Utah Juniper Pollen

NDC Code 49643-370-30
Proprietary Name Utah Juniper Pollen
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49643-370-30)
Product NDC 49643-370
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Juniperus osteosperma
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name JUNIPERUS OSTEOSPERMA 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 Utah Juniper Pollen


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