Levothyroxine Sodium

Product NDC

43063-422

11-digit product format

430630422

Labeler code

43063

Product ID

43063-422_77ce0203-96e1-79e1-e053-2a91aa0a282b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levothyroxine Sodium

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx 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

2019-12-31

Current FDA listing

Historical FDA.report record