All Day Pain Relief

Product NDC

55315-256

11-digit product format

553150256

Labeler code

55315

Product ID

55315-256_3e530af2-9f61-48e9-8474-5fd2134ee686

Type

HUMAN OTC DRUG

Nonproprietary name

Naproxen Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Freds Inc

Application

ANDA091353

Marketing category

ANDA

Marketing start

2014-08-31

Marketing end

2019-12-31

Substance

NAPROXEN SODIUM

Active strength

220 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record