NDC Code | 70511-111-10 |
Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (70511-111-10) > 5 mL in 1 VIAL, SINGLE-USE |
Product NDC | 70511-111 |
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 | 20181227 |
Marketing Category Name | ANDA |
Application Number | ANDA208749 |
Manufacturer | MAIA Pharmaceuticals, Inc. |
Substance Name | LEVOTHYROXINE SODIUM ANHYDROUS |
Strength | 100 |
Strength Unit | ug/5mL |
Pharmacy Classes | Thyroxine [CS], l-Thyroxine [EPC] |