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Short Ragweed Pollen - 36987-3453-4 - (Short Ragweed Pollen)

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Drug Information of Short Ragweed Pollen

Product NDC: 36987-3453
Proprietary Name: Short Ragweed Pollen
Non Proprietary Name: Short Ragweed Pollen
Active Ingredient(s): .1    g/mL & nbsp;   Short Ragweed Pollen
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Short Ragweed Pollen

Product NDC: 36987-3453
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102203
Marketing Category: BLA
Start Marketing Date: 19830408

Package Information of Short Ragweed Pollen

Package NDC: 36987-3453-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-3453-4)

NDC Information of Short Ragweed Pollen

NDC Code 36987-3453-4
Proprietary Name Short Ragweed Pollen
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-3453-4)
Product NDC 36987-3453
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Short Ragweed Pollen
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19830408
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name AMBROSIA ARTEMISIIFOLIA POLLEN
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes 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 Short Ragweed Pollen


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