Levothyroxine

Product NDC

51655-091

11-digit product format

516550091

Labeler code

51655

Product ID

51655-091_e561a5af-c541-4ef0-b027-9d1af884ac72

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levothyroxine

Dosage form

TABLET

Route

ORAL

Labeler

Northwind Pharmaceuticals, LLC

Application

NDA021342

Marketing category

NDA

Marketing start

2014-07-10

Marketing end

0000-00-00

Substance

LEVOTHYROXINE SODIUM

Active strength

25 ug/1

Pharmacologic classes

l-Thyroxine [EPC],Thyroxine [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record