FENOFIBRATE
- Product NDC
- 68180-745
- 11-digit product format
- 681800745
- Labeler code
- 68180
- Product ID
- 68180-745_7621f047-a55e-4b08-ab1a-fcd8a6d387bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- NDA021695
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-12-11
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 68180-745-06 | 68180074506 | 30 CAPSULE in 1 BOTTLE (68180-745-06) | 30 capsule | 2020-12-11 | 0000-00-00 | No | No | Current |