Diclofenac Sodium

Product NDC

71335-0170

11-digit product format

713350170

Labeler code

71335

Product ID

71335-0170_1aee9670-5654-48f4-a1bd-339501b0ddd9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac Sodium

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA076201

Marketing category

ANDA

Marketing start

2002-11-06

Marketing end

0000-00-00

Substance

DICLOFENAC SODIUM

Active strength

100 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

2019-12-31

Current FDA listing

Historical FDA.report record