All Day Pain Relief

Product NDC

37205-744

Type

HUMAN OTC DRUG

Nonproprietary name

Naproxen Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Cardinal Health (Leader) 37205

Application

ANDA079096

Marketing category

ANDA

Substance

NAPROXEN SODIUM

Current FDA listing

Historical FDA.report record