NDC 51655-143 – Gemfibrozil
Gemfibrozil 600 mg/1 · Tablet · Oral
Product NDC51655-143
Product details
- Brand name
- Gemfibrozil
- Generic name
- Gemfibrozil
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077836
- Marketed since
- August 14, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Gemfibrozil 600 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 51655-143-25 | 60 TABLET in 1 BOTTLE, PLASTIC (51655-143-25) | Dec 6, 2022 |
| 51655-143-26 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-143-26) | Aug 14, 2017 |
| 51655-143-52 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-143-52) | Nov 13, 2017 |
| 51655-143-83 | 180 TABLET in 1 BOTTLE, PLASTIC (51655-143-83) | Aug 14, 2017 |
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