Naproxen sodium

Product NDC

70518-0178

11-digit product format

705180178

Labeler code

70518

Product ID

70518-0178_82386071-1720-217f-e053-2991aa0a846c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Naproxen sodium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078486

Marketing category

ANDA

Marketing start

2017-01-25

Marketing end

0000-00-00

Substance

NAPROXEN SODIUM

Active strength

550 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record