FENOPROFEN CALCIUM

Product NDC
54288-132
11-digit product format
542880132
Labeler code
54288
Product ID
54288-132_a03faba1-e4b5-4c21-988a-64dbcf0d6a61
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FENOPROFEN CALCIUM
Dosage form
CAPSULE
Route
ORAL
Labeler
BPI Labs LLC
Application
NDA017604
Marketing category
NDA
Marketing start
2016-07-06
Marketing end
0000-00-00
Substance
FENOPROFEN CALCIUM
Active strength
400 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54288-132-092025-04-23C16284748780-19d75b9d0-15c1-f424-e053-dadaa90a57ce3028652a-56ee-497d-8f77-edba86ddf8cb
54288-132-092020-01-31C16284748780-19d75b9d0-15c1-f424-e053-dadaa90a57ce3028652a-56ee-497d-8f77-edba86ddf8cb

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
54288-132-09EA - Each54288-132d06badbb-7561-4545-b0bc-899587af08af12016-07-19