NDC 62135-838 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral
Product NDC62135-838
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Chartwell RX, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209660
- Marketed since
- February 11, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 62135-838-90 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-838-90) | Jul 5, 2024 |
Other Fenofibrate products
- 50090-3056 Fenofibrate 48 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-5796 Fenofibrate 145 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-3044 Fenofibrate 145 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7209 Fenofibrate 160 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7242 Fenofibrate 145 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7572 Fenofibrate 54 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6934 Fenofibrate 145 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7208 Fenofibrate 160 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 62332-350 Fenofibrate 54 mg/1 · Tablet, Film Coated · Alembic Pharmaceuticals Inc.
- 62332-361 Fenofibrate 145 mg/1 · Tablet, Film Coated · Alembic Pharmaceuticals Inc.
- 62332-351 Fenofibrate 160 mg/1 · Tablet, Film Coated · Alembic Pharmaceuticals Inc.
- 62332-360 Fenofibrate 48 mg/1 · Tablet, Film Coated · Alembic Pharmaceuticals Inc.