NDC 43598-745 – Ezetimibe and Simvastatin
Ezetimibe 10 mg/1; Simvastatin 80 mg/1 · Tablet · Oral
Product NDC43598-745
Product details
- Brand name
- Ezetimibe and Simvastatin
- Generic name
- Ezetimibe and Simvastatin
- Labeler
- Dr.Reddys Laboratories Inc
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA200909
- Marketed since
- November 20, 2018
- Marketing end
- November 30, 2026
- Pharmacologic class
- Dietary Cholesterol Absorption Inhibitor; HMG-CoA Reductase Inhibitor
Active ingredients
- Ezetimibe 10 mg/1
- Simvastatin 80 mg/1
Uses, dosage, side effects and warnings for Ezetimibe and simvastatin →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 43598-745-05 | 500 TABLET in 1 BOTTLE (43598-745-05) | Nov 20, 2018 |
| 43598-745-30 | 30 TABLET in 1 BOTTLE (43598-745-30) | Nov 20, 2018 |
| 43598-745-90 | 90 TABLET in 1 BOTTLE (43598-745-90) | Nov 20, 2018 |
Recalls mentioning this NDC
- D-0082-2022 Nov 10, 2021 · Class II
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity - D-0081-2022 Nov 10, 2021 · Class II
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity - D-0084-2022 Nov 10, 2021 · Class II
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity - D-0085-2022 Nov 10, 2021 · Class II
Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10… - D-0083-2022 Nov 10, 2021 · Class II
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
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