Diclofenac Sodium

Product NDC

66267-358

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA074514

Marketing category

ANDA

Substance

DICLOFENAC SODIUM

Current FDA listing

Historical FDA.report record