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Black Birch - 49288-0626-4 - (Black Birch)

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Drug Information of Black Birch

Product NDC: 49288-0626
Proprietary Name: Black Birch
Non Proprietary Name: Black Birch
Active Ingredient(s): .05    g/mL & nbsp;   Black Birch
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Black Birch

Product NDC: 49288-0626
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Black Birch

Package NDC: 49288-0626-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0626-4)

NDC Information of Black Birch

NDC Code 49288-0626-4
Proprietary Name Black Birch
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0626-4)
Product NDC 49288-0626
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Black Birch
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name BETULA LENTA POLLEN
Strength Number .05
Strength Unit 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]

Complete Information of Black Birch


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