All Day Pain Relief

Product NDC

49781-046

11-digit product format

497810046

Labeler code

49781

Product ID

49781-046_421e35be-c7fd-4b75-b74d-7939ac024300

Type

HUMAN OTC DRUG

Nonproprietary name

Naproxen Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Cardinal Health (Leader) 49781

Application

ANDA079096

Marketing category

ANDA

Marketing start

2012-06-25

Marketing end

2019-07-25

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