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Common Mugwort Sage - 49288-0495-4 - (Common Mugwort Sage)

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Drug Information of Common Mugwort Sage

Product NDC: 49288-0495
Proprietary Name: Common Mugwort Sage
Non Proprietary Name: Common Mugwort Sage
Active Ingredient(s): .05    g/mL & nbsp;   Common Mugwort Sage
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Common Mugwort Sage

Product NDC: 49288-0495
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19770909

Package Information of Common Mugwort Sage

Package NDC: 49288-0495-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0495-4)

NDC Information of Common Mugwort Sage

NDC Code 49288-0495-4
Proprietary Name Common Mugwort Sage
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0495-4)
Product NDC 49288-0495
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Common Mugwort 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 VULGARIS 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 Common Mugwort Sage


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