NDC 0904-6954 – Levothyroxine Sodium
Levothyroxine Sodium .112 mg/1 · Tablet · Oral
Product NDC0904-6954
Product details
- Brand name
- Levothyroxine Sodium
- Generic name
- Levothyroxine Sodium
- Labeler
- Major Pharmaceuticals
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209713
- Marketed since
- March 20, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- l-Thyroxine
Active ingredients
- Levothyroxine Sodium .112 mg/1
Uses, dosage, side effects and warnings for Levothyroxine Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0904-6954-61 | 100 BLISTER PACK in 1 CARTON (0904-6954-61) / 1 TABLET in 1 BLISTER PACK | Mar 20, 2019 |
Recalls mentioning this NDC
- D-0710-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0711-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0708-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0705-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0700-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0702-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0707-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0703-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0709-2026 Jul 29, 2026 · Class II
Subpotent Drug - D-0701-2026 Jul 29, 2026 · Class II
Subpotent Drug
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