TOLMETIN SODIUM

Product NDC

53489-506

11-digit product format

534890506

Labeler code

53489

Product ID

53489-506_e030ea24-4db5-4eb4-9dc5-b4397c29cb60

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

tolmetin sodium

Dosage form

TABLET

Route

ORAL

Labeler

Mutual Pharmaceutical Company, Inc.

Application

ANDA073311

Marketing category

ANDA

Marketing start

2009-09-04

Marketing end

0000-00-00

Substance

TOLMETIN SODIUM

Active strength

200 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record