Methocarb 500-EZS

Product NDC
59088-724
11-digit product format
590880724
Labeler code
59088
Product ID
59088-724_b3ca019e-98e0-1007-e053-2a95a90a1690
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
KIT
Labeler
PureTek Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2018-10-23
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2020-06-10 20:45 UTC · source 2020-06-10excluded productproduct59088-724EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage59088-72459088-724-00EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…

Additional Listing Data#

Finished product
Yes
Brand name base
Methocarb 500-EZS
Listing expiration
2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
197943Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
383ce408-1085-43e7-944e-957ff2a9d553Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
492965be-47bc-38cf-57c4-5c5e0343abe5Product name620211028
02a01e9c-3f4e-c0ee-6542-be865127aea3Product name820190205

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59088-724-00Methocarb 500-EZS1 in 1 KITKIT13
69543-134-10Methocarb 500-EZS100 in 1 BOTTLETABLET, FILM COATED100500 mg3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59088-724METHOCARB 500-EZS (METHOCARBAMOL) KIT [PURETEK CORPORATION]3Current NDC, Legacy NDC, 2 package rows20201114_383ce408-1085-43e7-944e-957ff2a9d553.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Methocarb 500-EZSMETHOCARBAMOLPureTek Corporation383ce408-1085-43e7-944e-957ff2a9d5532020-11-10Warnings, Adverse reactionsExact identifier
ndc (product): 59088-724

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197943methocarbamol 500 MG Oral TabletPSN383ce408-1085-43e7-944e-957ff2a9d5533
197943methocarbamol 500 MG Oral TabletSCD383ce408-1085-43e7-944e-957ff2a9d5533

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59088-724-00590880724001 KIT in 1 KIT (59088-724-00) * 100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10) 1 kit2018-10-230000-00-00NoNoCurrent
69543-134-1069543013410100 in 1 BOTTLEHistorical