Fenofibrate
- Product NDC
- 68084-835
- 11-digit product format
- 680840835
- Labeler code
- 68084
- Product ID
- 68084-835_e5e7f145-a218-06bc-e053-2a95a90a364b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075868
- Marketing category
- ANDA
- Marketing start
- 2014-09-23
- Marketing end
- 2023-01-31
- Substance
- FENOFIBRATE
- Active strength
- 134 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 |
|---|
| 68084-835-32 | 68084083532 | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-835-32) > 1 CAPSULE in 1 BLISTER PACK (68084-835-33) | 20 blister pack | 2014-09-23 | 0000-00-00 | No | No | Current |