NDC 68382-553 – Gemfibrozil
Gemfibrozil 600 mg/1 · Tablet · Oral
Product NDC68382-553
Product details
- Brand name
- Gemfibrozil
- Generic name
- Gemfibrozil
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204189
- Marketed since
- January 15, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Gemfibrozil 600 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 68382-553-01 | 100 TABLET in 1 BOTTLE (68382-553-01) | Jan 15, 2019 |
| 68382-553-05 | 500 TABLET in 1 BOTTLE (68382-553-05) | Jan 15, 2019 |
| 68382-553-06 | 30 TABLET in 1 BOTTLE (68382-553-06) | Jan 15, 2019 |
| 68382-553-10 | 1000 TABLET in 1 BOTTLE (68382-553-10) | Jan 15, 2019 |
| 68382-553-14 | 60 TABLET in 1 BOTTLE (68382-553-14) | Jan 15, 2019 |
| 68382-553-16 | 90 TABLET in 1 BOTTLE (68382-553-16) | Jan 15, 2019 |
| 68382-553-30 | 10 BLISTER PACK in 1 CARTON (68382-553-30) / 10 TABLET in 1 BLISTER PACK | Jan 15, 2019 |
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