All Day Pain Relief

Product NDC

37205-744

11-digit product format

372050744

Labeler code

37205

Product ID

37205-744_44de66ce-e61c-46db-8805-7669666d3a16

Type

HUMAN OTC DRUG

Nonproprietary name

Naproxen Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Cardinal Health (Leader) 37205

Application

ANDA079096

Marketing category

ANDA

Marketing start

2012-08-30

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