| NDC Code | 49281-752-21 |
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| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (49281-752-21) / 1 mL in 1 VIAL, MULTI-DOSE (49281-752-78) |
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| Product NDC | 49281-752 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tubersol |
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| Non-Proprietary Name | Tuberculin Purified Protein Derivative |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRADERMAL |
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| Start Marketing Date | 19560815 |
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| Marketing Category Name | BLA |
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| Application Number | BLA103941 |
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| Manufacturer | Sanofi Pasteur Inc. |
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| Substance Name | TUBERCULIN PURIFIED PROTEIN DERIVATIVE |
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| Strength | 5 |
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| Strength Unit | [iU]/.1mL |
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| Pharmacy Classes | Antigens, Bacterial [CS], Cell-mediated Immunity [PE], Skin Test Antigen [EPC], Tuberculosis Skin Test [EPC] |
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