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Poplar Mixture - 49288-0397-4 - (Poplar Mixture)

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Drug Information of Poplar Mixture

Product NDC: 49288-0397
Proprietary Name: Poplar Mixture
Non Proprietary Name: Poplar Mixture
Active Ingredient(s): .025; .025    g/mL; g/mL & nbsp;   Poplar Mixture
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Poplar Mixture

Product NDC: 49288-0397
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Poplar Mixture

Package NDC: 49288-0397-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0397-4)

NDC Information of Poplar Mixture

NDC Code 49288-0397-4
Proprietary Name Poplar Mixture
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0397-4)
Product NDC 49288-0397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Poplar Mixture
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name POPULUS ALBA POLLEN; POPULUS NIGRA POLLEN
Strength Number .025; .025
Strength Unit g/mL; 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],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 Poplar Mixture


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