Diclofenac Potassium

Product NDC

55289-781

11-digit product format

552890781

Labeler code

55289

Product ID

55289-781_8736e086-3abe-5523-e053-2991aa0ad3d8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA075229

Marketing category

ANDA

Marketing start

1998-11-20

Marketing end

2020-08-31

Substance

DICLOFENAC POTASSIUM

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

0000-00-00

Current FDA listing

Historical FDA.report record