NDC 68180-974 – Levothyroxine Sodium
Levothyroxine Sodium .175 mg/1 · Tablet · Oral
Product NDC68180-974
Product details
- Brand name
- Levothyroxine Sodium
- Generic name
- Levothyroxine Sodium
- Labeler
- Lupin Pharmaceuticals, Inc.
- 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 .175 mg/1
Uses, dosage, side effects and warnings for Levothyroxine Sodium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68180-974-01 | 100 TABLET in 1 BOTTLE (68180-974-01) | Mar 20, 2019 |
| 68180-974-03 | 1000 TABLET in 1 BOTTLE (68180-974-03) | Mar 20, 2019 |
| 68180-974-09 | 90 TABLET in 1 BOTTLE (68180-974-09) | Mar 20, 2019 |
Recalls mentioning this NDC
- D-0167-2025 Jan 8, 2025 · Class II
Failed Impurities/Degradation Specifications: Out of specifications result observed in the drug substance for impurity test during 3-month long term stability study.
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