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Short/Giant Ragweed Mixture - 49288-0454-3 - (Short/Giant Ragweed Mixture)

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Drug Information of Short/Giant Ragweed Mixture

Product NDC: 49288-0454
Proprietary Name: Short/Giant Ragweed Mixture
Non Proprietary Name: Short/Giant Ragweed Mixture
Active Ingredient(s): .025; .025    g/mL; g/mL & nbsp;   Short/Giant Ragweed Mixture
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Short/Giant Ragweed Mixture

Product NDC: 49288-0454
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Short/Giant Ragweed Mixture

Package NDC: 49288-0454-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0454-3)

NDC Information of Short/Giant Ragweed Mixture

NDC Code 49288-0454-3
Proprietary Name Short/Giant Ragweed Mixture
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0454-3)
Product NDC 49288-0454
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Short/Giant Ragweed Mixture
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 ARTEMISIIFOLIA POLLEN; AMBROSIA TRIFIDA POLLEN
Strength Number .025; .025
Strength Unit g/mL; g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient],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/Giant Ragweed Mixture


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