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