Naproxen Sodium

Product NDC
68788-6934
11-digit product format
687886934
Labeler code
68788
Product ID
68788-6934_569e3e31-2f72-4d83-9efe-6f7229072e0d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA078314
Marketing category
ANDA
Marketing start
2017-03-27
Marketing end
0000-00-00
Substance
NAPROXEN SODIUM
Active strength
550 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-6934-168788693401100 TABLET in 1 BOTTLE (68788-6934-1) 100 tablet2017-03-270000-00-00NoNoCurrent
68788-6934-26878869340220 TABLET in 1 BOTTLE (68788-6934-2) 20 tablet2017-03-270000-00-00NoNoCurrent
68788-6934-36878869340330 TABLET in 1 BOTTLE (68788-6934-3) 30 tablet2017-03-270000-00-00NoNoCurrent
68788-6934-46878869340414 TABLET in 1 BOTTLE (68788-6934-4) 14 tablet2017-03-270000-00-00NoNoCurrent
68788-6934-66878869340660 TABLET in 1 BOTTLE (68788-6934-6) 60 tablet2017-03-270000-00-00NoNoCurrent
68788-6934-868788693408120 TABLET in 1 BOTTLE (68788-6934-8) 120 tablet2017-03-270000-00-00NoNoCurrent
68788-6934-96878869340990 TABLET in 1 BOTTLE (68788-6934-9) 90 tablet2017-03-270000-00-00NoNoCurrent