NAPROXEN

Product NDC

68071-3345

11-digit product format

680713345

Labeler code

68071

Product ID

68071-3345_8cc89523-995d-c24e-e053-2a95a90abdc1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

NAPROXEN

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA091416

Marketing category

ANDA

Marketing start

2016-07-06

Marketing end

0000-00-00

Substance

NAPROXEN

Active strength

375 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