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Mulberry Mixture - 49288-0311-1 - (Mulberry Mixture)

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Drug Information of Mulberry Mixture

Product NDC: 49288-0311
Proprietary Name: Mulberry Mixture
Non Proprietary Name: Mulberry Mixture
Active Ingredient(s): .0167; .0167; .0167    g/mL; g/mL; g/mL & nbsp;   Mulberry Mixture
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mulberry Mixture

Product NDC: 49288-0311
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Mulberry Mixture

Package NDC: 49288-0311-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0311-1)

NDC Information of Mulberry Mixture

NDC Code 49288-0311-1
Proprietary Name Mulberry Mixture
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0311-1)
Product NDC 49288-0311
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mulberry 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 BROUSSONETIA PAPYRIFERA POLLEN; MORUS ALBA POLLEN; MORUS RUBRA POLLEN
Strength Number .0167; .0167; .0167
Strength Unit g/mL; 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],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 Mulberry Mixture


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