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Elm Mixture - 49288-0185-4 - (Elm Mixture)

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Drug Information of Elm Mixture

Product NDC: 49288-0185
Proprietary Name: Elm Mixture
Non Proprietary Name: Elm Mixture
Active Ingredient(s): .01; .01    g/mL; g/mL & nbsp;   Elm Mixture
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Elm Mixture

Product NDC: 49288-0185
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Elm Mixture

Package NDC: 49288-0185-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0185-4)

NDC Information of Elm Mixture

NDC Code 49288-0185-4
Proprietary Name Elm Mixture
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0185-4)
Product NDC 49288-0185
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Elm 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 ULMUS AMERICANA POLLEN; ULMUS PUMILA POLLEN
Strength Number .01; .01
Strength Unit g/mL; g/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],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 Elm Mixture


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