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Groundsel Tree - 49288-0076-2 - (Groundsel Tree)

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Drug Information of Groundsel Tree

Product NDC: 49288-0076
Proprietary Name: Groundsel Tree
Non Proprietary Name: Groundsel Tree
Active Ingredient(s): .05    g/mL & nbsp;   Groundsel Tree
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Groundsel Tree

Product NDC: 49288-0076
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Groundsel Tree

Package NDC: 49288-0076-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0076-2)

NDC Information of Groundsel Tree

NDC Code 49288-0076-2
Proprietary Name Groundsel Tree
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0076-2)
Product NDC 49288-0076
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Groundsel Tree
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name BACCHARIS HALIMIFOLIA 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 Groundsel Tree


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