Nalfon

Product NDC
71335-0805
11-digit product format
713350805
Labeler code
71335
Product ID
71335-0805_2d967825-a1a2-4ab6-a871-37d6f7fe9a29
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fenoprofen calcium
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA017604
Marketing category
NDA
Marketing start
2012-08-27
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0805-17133508050130 CAPSULE in 1 BOTTLE (71335-0805-1) 30 capsule2022-02-140000-00-00NoNoCurrent
71335-0805-27133508050260 CAPSULE in 1 BOTTLE (71335-0805-2) 60 capsule2022-02-140000-00-00NoNoCurrent
71335-0805-37133508050390 CAPSULE in 1 BOTTLE (71335-0805-3) 90 capsule2022-02-140000-00-00NoNoCurrent
71335-0805-471335080504120 CAPSULE in 1 BOTTLE (71335-0805-4) 120 capsule2022-02-140000-00-00NoNoCurrent
71335-0805-57133508050528 CAPSULE in 1 BOTTLE (71335-0805-5) 28 capsule2022-02-140000-00-00NoNoCurrent