| NDC Code | 63323-648-10 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-648-10) / 5 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 63323-648 |
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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 | 20110624 |
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| Marketing Category Name | NDA |
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| Application Number | NDA202231 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | LEVOTHYROXINE SODIUM ANHYDROUS |
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| Strength | 500 |
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| Strength Unit | ug/5mL |
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| Pharmacy Classes | Thyroxine [CS], l-Thyroxine [EPC] |
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