Liothyronine Sodium

Product NDC

68071-2133

11-digit product format

680712133

Labeler code

68071

Product ID

68071-2133_46f11a74-eb85-4ef8-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Liothyronine Sodium

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA090097

Marketing category

ANDA

Marketing start

2009-03-23

Marketing end

0000-00-00

Substance

LIOTHYRONINE SODIUM

Active strength

50 ug/1

Pharmacologic classes

l-Triiodothyronine [EPC],Triiodothyronine [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record