| NDC Code | 70860-451-10 |
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| Package Description | 1 VIAL in 1 CARTON (70860-451-10) / 5 mL in 1 VIAL |
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| Product NDC | 70860-451 |
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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 Anhydrous |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20181215 |
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| End Marketing Date | 20240731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208749 |
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| Manufacturer | Athenex Pharmaceutical Division, LLC. |
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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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