Liothyronine Sodium

Product NDC
0574-0222
11-digit product format
005740222
Labeler code
0574
Product ID
0574-0222_b2b6f867-bb3b-4156-bd9c-9183d0e12381
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Liothyronine Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Paddock Laboratories, LLC
Application
ANDA090097
Marketing category
ANDA
Marketing start
2009-03-23
Marketing end
2019-09-01
Substance
LIOTHYRONINE SODIUM
Active strength
25 ug/1
Pharmacologic classes
l-Triiodothyronine [EPC],Triiodothyronine [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b42496cd-a994-8ba1-597f-e507aa62246eProduct name520250116

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0574-0222-01EA - Each0574-0222c27d242d-68db-48f4-9f2b-34a1d6467c8b12012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
903697liothyronine sodium 25 MCG Oral TabletPSNfecd164d-1344-4d2f-97a7-ebe972470d2b2
903697liothyronine sodium 0.025 MG Oral TabletSCDfecd164d-1344-4d2f-97a7-ebe972470d2b2
903697liothyronine sodium 25 MCG Oral TabletSYfecd164d-1344-4d2f-97a7-ebe972470d2b2