Product NDC: | 54868-2972 |
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) |
Product NDC: | 54868-2972 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103941 |
Marketing Category: | BLA |
Start Marketing Date: | 19560815 |
Package NDC: | 54868-2972-1 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (54868-2972-1) > 1 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 54868-2972-1 |
Proprietary Name | TUBERSOL |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (54868-2972-1) > 1 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 54868-2972 |
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 | Physicians Total Care, 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] |