NDC 62756-591 – Liothyronine sodium
Liothyronine Sodium 50 ug/1 · Tablet · Oral
Product NDC62756-591
Product details
- Brand name
- Liothyronine sodium
- Generic name
- Liothyronine sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091382
- Marketed since
- November 28, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- l-Triiodothyronine
Active ingredients
- Liothyronine Sodium 50 ug/1
Uses, dosage, side effects and warnings for Liothyronine Sodium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 62756-591-01 | 90 TABLET in 1 BOTTLE (62756-591-01) | Jun 26, 2023 |
| 62756-591-08 | 100 TABLET in 1 BOTTLE (62756-591-08) | Nov 28, 2019 |
| 62756-591-18 | 1000 TABLET in 1 BOTTLE (62756-591-18) | Nov 28, 2019 |
| 62756-591-83 | 30 TABLET in 1 BOTTLE (62756-591-83) | Nov 28, 2019 |
| 62756-591-88 | 100 TABLET in 1 BOTTLE (62756-591-88) | Nov 28, 2019 |
Recalls mentioning this NDC
- D-0150-2024 Dec 20, 2023 · Class II
Failed Impurities/Degradation Specifications - D-0083-2024 Nov 8, 2023 · Class II
Failed Impurities/Degradation Specifications. - D-0084-2024 Nov 8, 2023 · Class II
Failed Impurities/Degradation Specifications.
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