NDC 65862-769 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet, Coated · Oral
Product NDC65862-769
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205118
- Marketed since
- May 5, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 145 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65862-769-01 | 100 TABLET, COATED in 1 BOTTLE (65862-769-01) | May 5, 2016 |
| 65862-769-05 | 500 TABLET, COATED in 1 BOTTLE (65862-769-05) | May 5, 2016 |
| 65862-769-78 | 10 BLISTER PACK in 1 CARTON (65862-769-78) / 10 TABLET, COATED in 1 BLISTER PACK (65862-769-10) | May 5, 2016 |
| 65862-769-90 | 90 TABLET, COATED in 1 BOTTLE (65862-769-90) | May 5, 2016 |
| 65862-769-99 | 1000 TABLET, COATED in 1 BOTTLE (65862-769-99) | May 5, 2016 |
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