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NDC 50090-1668-00 TUBERSOL 5 [iU]/.1mL Details
TUBERSOL 5 [iU]/.1mL
TUBERSOL is a INTRADERMAL INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is TUBERCULIN PURIFIED PROTEIN DERIVATIVE.
Product Information
| NDC | 50090-1668 |
|---|---|
| Product ID | 50090-1668_5471ed3d-e3c2-407e-b467-cc5a1c8be2fa |
| Associated GPIs | 94300070002010 |
| GCN Sequence Number | 009700 |
| GCN Sequence Number Description | tuberculin,purif.prot.deriv. VIAL 5 T/0.1 ML INTRADERM |
| HIC3 | W7T |
| HIC3 Description | ANTIGENIC SKIN TESTS |
| GCN | 44051 |
| HICL Sequence Number | 004227 |
| HICL Sequence Number Description | TUBERCULIN, PURIFIED PROTEIN DERIVATIVE |
| Brand/Generic | Generic |
| Proprietary Name | TUBERSOL |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Tuberculin Purified Protein Derivative |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRADERMAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | [iU]/.1mL |
| Substance Name | TUBERCULIN PURIFIED PROTEIN DERIVATIVE |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Antigens, Bacterial [CS], Cell-mediated Immunity [PE], Skin Test Antigen [EPC], Tuberculosis Skin Test [EPC] |
| DEA Schedule | n/a |
| Marketing Category | BLA |
| Application Number | BLA103941 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-1668-00 (50090166800)
| NDC Package Code | 50090-1668-0 |
|---|---|
| Billing NDC | 50090166800 |
| Package | 1 VIAL, MULTI-DOSE in 1 CARTON (50090-1668-0) / 5 mL in 1 VIAL, MULTI-DOSE |
| Marketing Start Date | 2015-01-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |