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Chestnut Oak - 49288-0641-5 - (Chestnut Oak)

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Drug Information of Chestnut Oak

Product NDC: 49288-0641
Proprietary Name: Chestnut Oak
Non Proprietary Name: Chestnut Oak
Active Ingredient(s): .05    g/mL & nbsp;   Chestnut Oak
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Chestnut Oak

Product NDC: 49288-0641
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Chestnut Oak

Package NDC: 49288-0641-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0641-5)

NDC Information of Chestnut Oak

NDC Code 49288-0641-5
Proprietary Name Chestnut Oak
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0641-5)
Product NDC 49288-0641
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chestnut Oak
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name QUERCUS MUEHLENBERGII 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 Chestnut Oak


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