Diclofenac Potassium

Product NDC

50090-0647

11-digit product format

500900647

Labeler code

50090

Product ID

50090-0647_9fd8f9b7-4bd3-448c-ab20-71bc8dab440f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA075229

Marketing category

ANDA

Marketing start

1998-11-20

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record