Sulindac

Product NDC

50090-0528

11-digit product format

500900528

Labeler code

50090

Product ID

50090-0528_f4c2c1c8-0ba0-42e1-9ef9-5982f3fc6ec3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sulindac

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA071795

Marketing category

ANDA

Marketing start

1990-04-03

Marketing end

0000-00-00

Substance

SULINDAC

Active strength

200 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