UNITHROID

Product NDC
0527-1373
11-digit product format
005271373
Labeler code
0527
Product ID
0527-1373_22c86d10-1b7b-448f-8004-1191fea738fa
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
levothyroxine sodium
Dosage form
TABLET
Route
ORAL
Labeler
Lannett Company, Inc.
Application
NDA021210
Marketing category
NDA
Marketing start
2000-08-21
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0527-1373-01EA - Each0527-13731ca77098-1a39-48b0-a6e1-4c889a38e0d412012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0527-1373-0100527137301100 TABLET in 1 BOTTLE, PLASTIC (0527-1373-01) 100 tablet2000-08-210000-00-00NoNoCurrent