NDC 42292-041 – Levothyroxine Sodium
Levothyroxine Sodium 137 ug/1 · Tablet · Oral
Product NDC42292-041
Product details
- Brand name
- Levothyroxine Sodium
- Generic name
- levothyroxine sodium
- Labeler
- Mylan Institutional Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076187
- Marketed since
- January 14, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- l-Thyroxine
Active ingredients
- Levothyroxine Sodium 137 ug/1
Uses, dosage, side effects and warnings for Levothyroxine Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 42292-041-20 | 100 BLISTER PACK in 1 CARTON (42292-041-20) / 1 TABLET in 1 BLISTER PACK (42292-041-01) | Jan 14, 2019 |
Recalls mentioning this NDC
- D-0136-2025 Dec 18, 2024 · Class II
Subpotent and Superpotent Drug - D-0132-2025 Dec 18, 2024 · Class II
Subpotent and Superpotent Drug - D-0134-2025 Dec 18, 2024 · Class II
Subpotent and Superpotent Drug
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