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