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Utah Juniper - 36987-2714-2 - (Utah Juniper)

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Drug Information of Utah Juniper

Product NDC: 36987-2714
Proprietary Name: Utah Juniper
Non Proprietary Name: Utah Juniper
Active Ingredient(s): .05    g/mL & nbsp;   Utah Juniper
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Utah Juniper

Product NDC: 36987-2714
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Utah Juniper

Package NDC: 36987-2714-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-2714-2)

NDC Information of Utah Juniper

NDC Code 36987-2714-2
Proprietary Name Utah Juniper
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-2714-2)
Product NDC 36987-2714
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Utah Juniper
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name JUNIPERUS OSTEOSPERMA POLLEN
Strength Number .05
Strength Unit g/mL
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


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