NDC 62332-351 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral
Product NDC62332-351
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Alembic Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213252
- Marketed since
- January 23, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 62332-351-30 | 30 TABLET, FILM COATED in 1 BOTTLE (62332-351-30) | Jan 23, 2020 |
| 62332-351-71 | 500 TABLET, FILM COATED in 1 BOTTLE (62332-351-71) | Jan 23, 2020 |
| 62332-351-90 | 90 TABLET, FILM COATED in 1 BOTTLE (62332-351-90) | Jan 23, 2020 |
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