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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70199-013-302021-02-01C16284748780-1ba0f9c33-27c4-a910-e053-dadaa90a0b85de93ca37-e911-4520-b6b4-437aba03ae70
70199-013-302021-01-29C16284748780-1ba0f9c33-27c4-a910-e053-dadaa90a0b85de93ca37-e911-4520-b6b4-437aba03ae70

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70199-013-30EA - Each70199-0135e4af388-ae97-4a46-8e7d-f0bdb6552a0212017-03-06