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Desert Ragweed - 49288-0455-3 - (Desert Ragweed)

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Drug Information of Desert Ragweed

Product NDC: 49288-0455
Proprietary Name: Desert Ragweed
Non Proprietary Name: Desert Ragweed
Active Ingredient(s): .05    g/mL & nbsp;   Desert Ragweed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Desert Ragweed

Product NDC: 49288-0455
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Desert Ragweed

Package NDC: 49288-0455-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0455-3)

NDC Information of Desert Ragweed

NDC Code 49288-0455-3
Proprietary Name Desert Ragweed
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0455-3)
Product NDC 49288-0455
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desert 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 DUMOSA 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 Desert Ragweed


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