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Acacia Pollen - 49288-0014-3 - (Acacia Pollen)

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Drug Information of Acacia Pollen

Product NDC: 49288-0014
Proprietary Name: Acacia Pollen
Non Proprietary Name: Acacia Pollen
Active Ingredient(s): .05    g/mL & nbsp;   Acacia Pollen
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Acacia Pollen

Product NDC: 49288-0014
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740423

Package Information of Acacia Pollen

Package NDC: 49288-0014-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0014-3)

NDC Information of Acacia Pollen

NDC Code 49288-0014-3
Proprietary Name Acacia Pollen
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0014-3)
Product NDC 49288-0014
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acacia Pollen
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740423
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ACACIA BAILEYANA 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 Acacia Pollen


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