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Western Ragweed - 36987-3434-3 - (Western Ragweed)

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Drug Information of Western Ragweed

Product NDC: 36987-3434
Proprietary Name: Western Ragweed
Non Proprietary Name: Western Ragweed
Active Ingredient(s): .05    g/mL & nbsp;   Western Ragweed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Western Ragweed

Product NDC: 36987-3434
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Western Ragweed

Package NDC: 36987-3434-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-3434-3)

NDC Information of Western Ragweed

NDC Code 36987-3434-3
Proprietary Name Western Ragweed
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-3434-3)
Product NDC 36987-3434
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Western Ragweed
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name AMBROSIA PSILOSTACHYA POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Western Ragweed


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