Fenoprofen Calcium

Product NDC
71335-0307
11-digit product format
713350307
Labeler code
71335
Product ID
71335-0307_209fdde4-6ab5-4b64-8d03-4a8078b76946
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fenoprofen calcium
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA017604
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2016-05-19
Marketing end
0000-00-00
Substance
FENOPROFEN CALCIUM
Active strength
400 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0307-3EA - Each71335-0307d73a015f-3d5b-4c6e-805e-8c2bb488d74212018-09-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0307-17133503070130 CAPSULE in 1 BOTTLE (71335-0307-1) 30 capsule2022-02-090000-00-00NoNoCurrent
71335-0307-27133503070260 CAPSULE in 1 BOTTLE (71335-0307-2) 60 capsule2022-02-090000-00-00NoNoCurrent
71335-0307-37133503070390 CAPSULE in 1 BOTTLE (71335-0307-3) 90 capsule2018-03-210000-00-00NoNoCurrent
71335-0307-471335030704120 CAPSULE in 1 BOTTLE (71335-0307-4) 120 capsule2022-02-090000-00-00NoNoCurrent
71335-0307-57133503070528 CAPSULE in 1 BOTTLE (71335-0307-5) 28 capsule2022-02-090000-00-00NoNoCurrent