TUBERSOL - 49281-752-22 - (Tuberculin Purified Protein Derivative)

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Drug Information of TUBERSOL

Product NDC: 49281-752
Proprietary Name: TUBERSOL
Non Proprietary Name: Tuberculin Purified Protein Derivative
Active Ingredient(s): 5    [iU]/.1mL & nbsp;   Tuberculin Purified Protein Derivative
Administration Route(s): INTRADERMAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of TUBERSOL

Product NDC: 49281-752
Labeler Name: Sanofi Pasteur Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103941
Marketing Category: BLA
Start Marketing Date: 19560815

Package Information of TUBERSOL

Package NDC: 49281-752-22
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (49281-752-22) > 5 mL in 1 VIAL, MULTI-DOSE (49281-752-98)

NDC Information of TUBERSOL

NDC Code 49281-752-22
Proprietary Name TUBERSOL
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (49281-752-22) > 5 mL in 1 VIAL, MULTI-DOSE (49281-752-98)
Product NDC 49281-752
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tuberculin Purified Protein Derivative
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL
Start Marketing Date 19560815
Marketing Category Name BLA
Labeler Name Sanofi Pasteur Inc.
Substance Name TUBERCULIN PURIFIED PROTEIN DERIVATIVE
Strength Number 5
Strength Unit [iU]/.1mL
Pharmaceutical Classes Skin Test Antigen [EPC],Tuberculosis Skin Test [EPC],Cell-mediated Immunity [PE],Antigens, Bacterial [Chemical/Ingredient]

Complete Information of TUBERSOL


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