FDA.reportPublic FDA data

Carisoprodol

Product NDC
51655-376
11-digit product format
516550376
Labeler code
51655
Product ID
51655-376_f81393a1-0bb9-47de-bab6-0c06c0daab8d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carisoprodol
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA040755
Marketing category
ANDA
Marketing start
2014-06-01
Marketing end
0000-00-00
Substance
CARISOPRODOL
Active strength
350 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
780d53a1-1665-e26e-d112-85333c0c8a2eProduct name520220516
2a21311a-89e2-0e83-2ebd-117f9798b2b2Product name120140508
9007e8a7-ff50-f9b9-7945-f2a1deadd94eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-376-522026-01-08C16284748780-19d75b9d0-f7ba-f424-e053-dadaa90a57ce3197e424-ac97-4667-b64d-503581f5edc1
51655-376-522020-01-31C16284748780-19d75b9d0-f7ba-f424-e053-dadaa90a57ce3197e424-ac97-4667-b64d-503581f5edc1

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CARISOPRODOLACTIVE INGREDIENT21925K482HCARISOPRODOL TABLET [NORTHWIND PHARMACEUTICALS]1
CARISOPRODOLACTIVE MOIETY21925K482HCARISOPRODOL TABLET [NORTHWIND PHARMACEUTICALS]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-376CARISOPRODOL TABLET [NORTHWIND PHARMACEUTICALS]1Legacy NDC20140618_3197e424-ac97-4667-b64d-503581f5edc1.zip