Diclofenac Sodium

Product NDC

66267-358

11-digit product format

662670358

Labeler code

66267

Product ID

66267-358_9cac56e5-d099-4990-e053-2995a90afd0c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA074514

Marketing category

ANDA

Marketing start

1996-03-26

Marketing end

0000-00-00

Substance

DICLOFENAC SODIUM

Active strength

50 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record