Naproxen Sodium

Product NDC
68788-7367
11-digit product format
687887367
Labeler code
68788
Product ID
68788-7367_98a8a6b9-61b7-4af6-811a-578c36a1f5be
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA090545
Marketing category
ANDA
Marketing start
2018-02-14
Marketing end
0000-00-00
Substance
NAPROXEN SODIUM
Active strength
220 mg/1
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
68788-7367-168788736701100 TABLET in 1 BOTTLE (68788-7367-1) 100 tablet2018-02-140000-00-00NoNoCurrent
68788-7367-26878873670220 TABLET in 1 BOTTLE (68788-7367-2) 20 tablet2018-02-140000-00-00NoNoCurrent
68788-7367-36878873670330 TABLET in 1 BOTTLE (68788-7367-3) 30 tablet2018-02-140000-00-00NoNoCurrent
68788-7367-46878873670440 TABLET in 1 BOTTLE (68788-7367-4) 40 tablet2018-02-140000-00-00NoNoCurrent
68788-7367-66878873670660 TABLET in 1 BOTTLE (68788-7367-6) 60 tablet2018-02-140000-00-00NoNoCurrent
68788-7367-868788736708120 TABLET in 1 BOTTLE (68788-7367-8) 120 tablet2018-02-140000-00-00NoNoCurrent
68788-7367-96878873670990 TABLET in 1 BOTTLE (68788-7367-9) 90 tablet2018-02-140000-00-00NoNoCurrent