All Day Pain Relief

Product NDC
55315-168
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Freds Inc
Application
ANDA079096
Marketing category
ANDA
Substance
NAPROXEN SODIUM
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
55315-168-241 BOTTLE, PLASTIC in 1 BOX (55315-168-24) > 24 TABLET in 1 BOTTLE, PLASTIC2015-09-302024-04-26NoCurrent