Levothyroxine Sodium

Product NDC

10544-257

11-digit product format

105440257

Labeler code

10544

Product ID

10544-257_1221646b-ea76-1ce9-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levothyroxine Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Blenheim Pharmacal, Inc.

Application

NDA021210

Marketing category

NDA

Marketing start

2013-11-18

Marketing end

0000-00-00

Substance

LEVOTHYROXINE SODIUM

Active strength

0 mg/1

Pharmacologic classes

l-Thyroxine [EPC],Thyroxine [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record