Levothyroxine Sodium

Product NDC

21695-756

11-digit product format

216950756

Labeler code

21695

Product ID

21695-756_3d43dfcf-f3b1-48a5-837c-d8010d45e0f0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levothyroxine Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Rebel Distributors Corp.

Application

NDA021210

Marketing category

NDA

Marketing start

2003-12-01

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