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Coastal Maple - 49288-0307-3 - (Coastal Maple)

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Drug Information of Coastal Maple

Product NDC: 49288-0307
Proprietary Name: Coastal Maple
Non Proprietary Name: Coastal Maple
Active Ingredient(s): .05    g/mL & nbsp;   Coastal Maple
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Coastal Maple

Product NDC: 49288-0307
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Coastal Maple

Package NDC: 49288-0307-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0307-3)

NDC Information of Coastal Maple

NDC Code 49288-0307-3
Proprietary Name Coastal Maple
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0307-3)
Product NDC 49288-0307
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Coastal Maple
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ACER MACROPHYLLUM POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE]

Complete Information of Coastal Maple


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