NDC 70771-1109 – Ezetimibe
Ezetimibe 10 mg/1 · Tablet · Oral
Product NDC70771-1109
Product details
- Brand name
- Ezetimibe
- Generic name
- Ezetimibe
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204331
- Marketed since
- August 9, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Dietary Cholesterol Absorption Inhibitor
Active ingredients
- Ezetimibe 10 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1109-0 | 1000 TABLET in 1 BOTTLE (70771-1109-0) | Aug 9, 2017 |
| 70771-1109-1 | 100 TABLET in 1 BOTTLE (70771-1109-1) | Aug 9, 2017 |
| 70771-1109-3 | 30 TABLET in 1 BOTTLE (70771-1109-3) | Aug 9, 2017 |
| 70771-1109-4 | 10 BLISTER PACK in 1 CARTON (70771-1109-4) / 10 TABLET in 1 BLISTER PACK (70771-1109-2) | Aug 9, 2017 |
| 70771-1109-5 | 500 TABLET in 1 BOTTLE (70771-1109-5) | Aug 9, 2017 |
| 70771-1109-9 | 90 TABLET in 1 BOTTLE (70771-1109-9) | Aug 9, 2017 |
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