NDC 70511-112 – Levothyroxine Sodium
Levothyroxine Sodium Anhydrous 200 ug/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC70511-112
Product details
- Brand name
- Levothyroxine Sodium
- Generic name
- Levothyroxine Sodium Anhydrous
- Labeler
- MAIA Pharmaceuticals, Inc.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA208749
- Marketed since
- December 27, 2018
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 70511-112-10 | 1 VIAL, SINGLE-USE in 1 CARTON (70511-112-10) / 5 mL in 1 VIAL, SINGLE-USE | Dec 27, 2018 |
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