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Desert Sage - 49288-0496-1 - (Desert Sage)

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Drug Information of Desert Sage

Product NDC: 49288-0496
Proprietary Name: Desert Sage
Non Proprietary Name: Desert Sage
Active Ingredient(s): .1    g/mL & nbsp;   Desert Sage
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Desert Sage

Product NDC: 49288-0496
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of Desert Sage

Package NDC: 49288-0496-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0496-1)

NDC Information of Desert Sage

NDC Code 49288-0496-1
Proprietary Name Desert Sage
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0496-1)
Product NDC 49288-0496
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desert Sage
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ARTEMISIA TRIDENTATA POLLEN
Strength Number .1
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 Desert Sage


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