Levothyroxine Sodium

Product NDC
21695-751
11-digit product format
216950751
Labeler code
21695
Product ID
21695-751_1f2e9f8f-0662-4fd4-b53c-776b6a395a30
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levothyroxine Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Rebel Distributors Corp
Application
NDA021210
Marketing category
NDA
Marketing start
2003-12-01
Marketing end
0000-00-00
Substance
LEVOTHYROXINE SODIUM
Active strength
0 mg/1
Pharmacologic classes
l-Thyroxine [EPC],Thyroxine [CS]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
97c252d3-9bb8-4530-bb44-9824dc7cf556Product name620250729
6c43b71c-35e6-4db3-ba24-c6ef42ff7003Product name320240207
890fd4bf-1a80-42b7-be1b-2d0259d5f0c8Product name520240207
c8ad26bf-af73-460b-b74e-1eff16cc4f9fProduct name520240207
01383843-4069-43cf-aa76-dc17a6f9f8c4Product name220230123
978cca7d-a938-4791-8322-da48d90a63efProduct name120230113
65f86ba3-8816-4e12-899b-18290c8de551Product name220210614
f16ab90f-08c2-40be-a543-66d9827cd1f3Product name120210601
6a33ec05-2ae2-45e5-ab82-2d94b3303923Product name120190709
93355a10-1c44-4c92-a11d-7d995e0200d9Product name120190219

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21695-751-302019-09-24C16284748780-1934fe258-4aaf-48b1-e053-8cdaa90a720aLevothyroxine Sodium Tablets, USP
21695-751-902019-09-24C16284748780-1934fe258-4aaf-48b1-e053-8cdaa90a720aLevothyroxine Sodium Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21695-751-30Levothyroxine Sodium30 in 1 BOTTLE, PLASTICTABLET301
21695-751-90Levothyroxine Sodium90 in 1 BOTTLE, PLASTICTABLET901

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-751-30EA - Each21695-751839edb17-939f-4709-b9d7-13840daabf9c12012-07-24
21695-751-90EA - Each21695-7515ae4d7de-8adf-455d-9937-8d79a5347a7012012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21695-751LEVOTHYROXINE SODIUM TABLET [REBEL DISTRIBUTORS CORP]1Legacy NDC, 2 package rows20110706_1f2e9f8f-0662-4fd4-b53c-776b6a395a30.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
966248levothyroxine sodium 112 MCG Oral TabletPSN1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966270levothyroxine sodium 137 MCG Oral TabletPSN1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966249levothyroxine sodium 175 MCG Oral TabletPSN1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966253levothyroxine sodium 88 MCG Oral TabletPSN1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966253levothyroxine sodium 0.088 MG Oral TabletSCD1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966248levothyroxine sodium 0.112 MG Oral TabletSCD1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966270levothyroxine sodium 0.137 MG Oral TabletSCD1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966249levothyroxine sodium 0.175 MG Oral TabletSCD1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966248levothyroxine sodium 112 MCG Oral TabletSY1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966270levothyroxine sodium 137 MCG Oral TabletSY1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966249levothyroxine sodium 175 MCG Oral TabletSY1f2e9f8f-0662-4fd4-b53c-776b6a395a301
966253levothyroxine sodium 88 MCG Oral TabletSY1f2e9f8f-0662-4fd4-b53c-776b6a395a301

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
21695-751-302169507513030 in 1 BOTTLE, PLASTICHistorical
21695-751-902169507519090 in 1 BOTTLE, PLASTICHistorical