Levothyroxine Sodium 70710-1835
Product NDC
70710-1835- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA217066
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Levothyroxine Sodium Anhydrous | 500 ug/5mL |
Drug Class
Thyroxine [CS]l-Thyroxine [EPC]
Packaging Options(1)
1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1835-1) / 5 mL in 1 VIAL, SINGLE-DOSE