Diclofenac Potassium

Product NDC

68071-4042

11-digit product format

680714042

Labeler code

68071

Product ID

68071-4042_56692e8a-05da-5fd3-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

diclofenac potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA075463

Marketing category

ANDA

Marketing start

1999-09-17

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