Levothyroxine Sodium

Product NDC

42023-161

11-digit product format

420230161

Labeler code

42023

Product ID

42023-161_7ebde671-a1ae-4b52-9307-f453fb0233c6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levothyroxine Sodium Anhydrous

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Par Pharmaceutical Companies, Inc.

Application

ANDA205366

Marketing category

ANDA

Marketing start

2015-12-11

Marketing end

0000-00-00

Substance

LEVOTHYROXINE SODIUM ANHYDROUS

Active strength

200 ug/5mL

Pharmacologic classes

l-Thyroxine [EPC],Thyroxine [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record