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Burweed Marsh Elder - 36987-3249-3 - (Burweed Marsh Elder)

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Drug Information of Burweed Marsh Elder

Product NDC: 36987-3249
Proprietary Name: Burweed Marsh Elder
Non Proprietary Name: Burweed Marsh Elder
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Burweed Marsh Elder
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Burweed Marsh Elder

Product NDC: 36987-3249
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Burweed Marsh Elder

Package NDC: 36987-3249-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-3249-3)

NDC Information of Burweed Marsh Elder

NDC Code 36987-3249-3
Proprietary Name Burweed Marsh Elder
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-3249-3)
Product NDC 36987-3249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Burweed Marsh Elder
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name IVA XANTHIFOLIA POLLEN
Strength Number 40000
Strength Unit [PNU]/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 Burweed Marsh Elder


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