| NDC Code | 63323-649-07 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-649-07) / 5 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 63323-649 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Levothyroxine Sodium |
|---|
| Non-Proprietary Name | Levothyroxine Sodium Anhydrous |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20110624 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA202231 |
|---|
| Manufacturer | Fresenius Kabi USA, LLC |
|---|
| Substance Name | LEVOTHYROXINE SODIUM ANHYDROUS |
|---|
| Strength | 100 |
|---|
| Strength Unit | ug/5mL |
|---|
| Pharmacy Classes | Thyroxine [CS], l-Thyroxine [EPC] |
|---|