NDC 0115-1325 – Fenofibric Acid
Fenofibric Acid 135 mg/1 · Capsule, Delayed Release · Oral
Product NDC0115-1325
Product details
- Brand name
- Fenofibric Acid
- Generic name
- Fenofibric Acid
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA200264
- Marketed since
- June 1, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibric Acid 135 mg/1
Uses, dosage, side effects and warnings for Fenofibric acid →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0115-1325-10 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1325-10) | Jun 1, 2024 |
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