LIPOFEN
- Product NDC
- 66869-137
- 11-digit product format
- 668690137
- Labeler code
- 66869
- Product ID
- 66869-137_dca82561-5635-4ef8-a622-66076c6c62d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Kowa Pharmaceuticals America, Inc.
- Application
- NDA021612
- Marketing category
- NDA
- Marketing start
- 2007-10-01
- Marketing end
- 2023-05-31
- Substance
- FENOFIBRATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66869-137-20 | 66869013720 | 30 CAPSULE in 1 BOTTLE, PLASTIC (66869-137-20) | 30 capsule | 2007-10-01 | 0000-00-00 | No | No | Current |
| 66869-137-30 | 66869013730 | 90 CAPSULE in 1 BOTTLE, PLASTIC (66869-137-30) | 90 capsule | 2007-10-01 | 0000-00-00 | No | No | Current |