NDC 0378-1821 – Levothyroxine Sodium
Levothyroxine Sodium 300 ug/1 · Tablet · Oral
Product NDC0378-1821
Product details
- Brand name
- Levothyroxine Sodium
- Generic name
- levothyroxine sodium
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076187
- Marketed since
- November 1, 2002
- Listing expires
- December 31, 2026
- Pharmacologic class
- l-Thyroxine
Active ingredients
- Levothyroxine Sodium 300 ug/1
Uses, dosage, side effects and warnings for Levothyroxine Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0378-1821-77 | 90 TABLET in 1 BOTTLE, PLASTIC (0378-1821-77) | May 27, 2016 |
Recalls mentioning this NDC
- D-0128-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0119-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0123-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0124-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0121-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0122-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0126-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0125-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0120-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained - D-0127-2025 Dec 18, 2024 · Class II
Superpotent Drug and Subpotent Drug: potency failures obtained
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