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Leaf Tobacco - 49288-0581-1 - (Leaf Tobacco)

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Drug Information of Leaf Tobacco

Product NDC: 49288-0581
Proprietary Name: Leaf Tobacco
Non Proprietary Name: Leaf Tobacco
Active Ingredient(s): .1    g/mL & nbsp;   Leaf Tobacco
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Leaf Tobacco

Product NDC: 49288-0581
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of Leaf Tobacco

Package NDC: 49288-0581-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0581-1)

NDC Information of Leaf Tobacco

NDC Code 49288-0581-1
Proprietary Name Leaf Tobacco
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0581-1)
Product NDC 49288-0581
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Leaf Tobacco
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name TOBACCO LEAF
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient]

Complete Information of Leaf Tobacco


General Information