NDC 63323-648 – Levothyroxine Sodium
Levothyroxine Sodium Anhydrous 500 ug/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC63323-648
Product details
- Brand name
- Levothyroxine Sodium
- Generic name
- Levothyroxine Sodium Anhydrous
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- NDA · NDA202231
- Marketed since
- June 24, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- l-Thyroxine
Active ingredients
- Levothyroxine Sodium Anhydrous 500 ug/5mL
Uses, dosage, side effects and warnings for Levothyroxine Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 63323-648-10 | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-648-10) / 5 mL in 1 VIAL, SINGLE-DOSE | Jun 24, 2011 |
| 63323-648-94 | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-648-94) / 5 mL in 1 VIAL, SINGLE-DOSE | Jun 24, 2011 |
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