All Day Relief

Product NDC

0536-1022

11-digit product format

005361022

Labeler code

0536

Product ID

0536-1022_8b0b968a-70e3-4f6d-af0e-6e78345d4545

Type

HUMAN OTC DRUG

Nonproprietary name

Naproxen Sodium, Coated Tablets

Dosage form

TABLET

Route

ORAL

Labeler

Rugby Laboratories

Application

ANDA090545

Marketing category

ANDA

Marketing start

2014-03-10

Marketing end

0000-00-00

Substance

NAPROXEN SODIUM

Active strength

220 mg/1

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record