Diclofenac Sodium

Product NDC

55700-127

11-digit product format

557000127

Labeler code

55700

Product ID

55700-127_bc1e70bb-e79f-4eae-8ca6-d55cfb7fbbc2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA074514

Marketing category

ANDA

Marketing start

1996-03-26

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