Etodolac

Product NDC

50090-1317

11-digit product format

500901317

Labeler code

50090

Product ID

50090-1317_dc0f426e-5c71-4c8b-bb27-55866209a86a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Etodolac

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA091134

Marketing category

ANDA

Marketing start

2014-02-15

Marketing end

0000-00-00

Substance

ETODOLAC

Active strength

600 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],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