Levothyroxine Sodium

Product NDC

68071-4735

11-digit product format

680714735

Labeler code

68071

Product ID

68071-4735_87dc077b-2c63-522b-e053-2995a90a68bc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levothyroxine Sodium

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record