TRIGLIDE
- Product NDC
- 70199-013
- 11-digit product format
- 701990013
- Labeler code
- 70199
- Product ID
- 70199-013_8fa31c95-612a-444a-b386-4f65e8e5a9a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Casper Pharma LLC
- Application
- NDA021350
- Marketing category
- NDA
- Marketing start
- 2017-02-01
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#