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Coastal Sage - 49288-0489-5 - (Coastal Sage)

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Drug Information of Coastal Sage

Product NDC: 49288-0489
Proprietary Name: Coastal Sage
Non Proprietary Name: Coastal Sage
Active Ingredient(s): .05    g/mL & nbsp;   Coastal Sage
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Coastal Sage

Product NDC: 49288-0489
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19770909

Package Information of Coastal Sage

Package NDC: 49288-0489-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0489-5)

NDC Information of Coastal Sage

NDC Code 49288-0489-5
Proprietary Name Coastal Sage
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0489-5)
Product NDC 49288-0489
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Coastal Sage
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19770909
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ARTEMISIA CALIFORNICA POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Coastal Sage


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