CARISOPRODOL

Product NDC
82868-062
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CARISOPRODOL
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Health Company, LLC
Application
ANDA203374
Marketing category
ANDA
Substance
CARISOPRODOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
82868-062-3030 TABLET in 1 BOTTLE, PLASTIC (82868-062-30) 2024-08-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CARISOPRODOLNorthwind Health Company, LLC2025-12-26HUMAN PRESCRIPTION DRUG LABEL2