NDC 70710-1834 – Levothyroxine Sodium
Levothyroxine Sodium Anhydrous 200 ug/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC70710-1834
Product details
- Brand name
- Levothyroxine Sodium
- Generic name
- levothyroxine sodium
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA217066
- Marketed since
- November 1, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- l-Thyroxine
Active ingredients
- Levothyroxine Sodium Anhydrous 200 ug/5mL
Uses, dosage, side effects and warnings for Levothyroxine Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1834-1 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1834-1) / 5 mL in 1 VIAL, SINGLE-DOSE | Nov 1, 2024 |
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