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False Ragweed - 49288-0204-5 - (False Ragweed)

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Drug Information of False Ragweed

Product NDC: 49288-0204
Proprietary Name: False Ragweed
Non Proprietary Name: False Ragweed
Active Ingredient(s): .05    g/mL & nbsp;   False Ragweed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of False Ragweed

Product NDC: 49288-0204
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of False Ragweed

Package NDC: 49288-0204-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0204-5)

NDC Information of False Ragweed

NDC Code 49288-0204-5
Proprietary Name False Ragweed
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0204-5)
Product NDC 49288-0204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name False Ragweed
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name AMBROSIA ACANTHICARPA 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 False Ragweed


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