Liothyronine Sodium

Product NDC

63629-7002

11-digit product format

636297002

Labeler code

63629

Product ID

63629-7002_21dd8fb2-fbec-4b43-963e-5af05aeb0b39

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Liothyronine Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA090097

Marketing category

ANDA

Marketing start

2009-03-23

Marketing end

0000-00-00

Substance

LIOTHYRONINE SODIUM

Active strength

25 ug/1

Pharmacologic classes

l-Triiodothyronine [EPC],Triiodothyronine [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record