Diclofenac Sodium

Product NDC

63629-1534

11-digit product format

636291534

Labeler code

63629

Product ID

63629-1534_455bef84-be0c-4e9f-913b-4bb3c62cfabf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA075185

Marketing category

ANDA

Marketing start

1998-11-13

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

2019-12-31

Current FDA listing

Historical FDA.report record