| NDC Code | 70710-1833-1 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1833-1) / 5 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 70710-1833 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Levothyroxine Sodium |
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| Non-Proprietary Name | Levothyroxine Sodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20241101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA217066 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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| Substance Name | LEVOTHYROXINE SODIUM ANHYDROUS |
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| Strength | 100 |
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| Strength Unit | ug/5mL |
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| Pharmacy Classes | Thyroxine [CS], l-Thyroxine [EPC] |
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