NDC 80425-0283-01 - Methocarbamol

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
80425-0283
Requested NDC
80425-0283-01
Package NDCs from labels
80425-0283-1, 80425-0283-2, 80425-0283-3, 80425-0283-4, 80425-0283-5, 80425-0283-01
Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC
Effective date
2024-12-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Methocarbamol - Advanced Rx Pharmacy of Tennessee, LLCAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80425-0283-1Methocarbamol30 in 1 BOTTLETABLET303
80425-0283-2Methocarbamol60 in 1 BOTTLETABLET603
80425-0283-3Methocarbamol90 in 1 BOTTLETABLET903
80425-0283-4Methocarbamol120 in 1 BOTTLETABLET1203
80425-0283-5Methocarbamol180 in 1 BOTTLETABLET1803

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80425-0283METHOCARBAMOL TABLET [ADVANCED RX PHARMACY OF TENNESSEE, LLC]3Current NDC, 5 package rows20250102_f6567e04-12f0-fa79-e053-2995a90a9a0e.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
80425-0283-1EA - Each80425-028321ad4035-e96c-4ea2-a554-99e52baa97dd12023-06-06
80425-0283-2EA - Each80425-0283da3849c3-560f-4914-82be-2a14544bd65212023-06-06
80425-0283-3EA - Each80425-028360d3fd48-4241-4935-8761-e177eff960f412023-06-06
80425-0283-4EA - Each80425-028328f053be-6da2-4ae5-967e-cbb4ac58f89112023-06-06
80425-0283-5EA - Each80425-028316bef713-1136-4b15-bf56-71d8bab14efe12023-06-06

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 9 of 9 · 171 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MethocarbamolMETHOCARBAMOLProficient Rx LP39b4362e-a26e-49cb-9d06-898bc9b0e0052021-04-01Warnings, Adverse reactionsExact identifier
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLSagent Pharmaceuticalsbc925726-4949-4647-bce8-e1180d36abe42021-03-12Warnings, Adverse reactionsExact identifier
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLProficient Rx LP75b964b7-3e76-4460-9777-7656b5daa32e2020-12-01Warnings, Adverse reactionsExact identifier
rxcui: 197943
unii: 125OD7737X
Methocarb 500-EZSMETHOCARBAMOLPureTek Corporation383ce408-1085-43e7-944e-957ff2a9d5532020-11-10Warnings, Adverse reactionsExact identifier
rxcui: 197943
methocarbamolMETHOCARBAMOLBaxter Healthcare Corporationa7f70b19-75ba-4e3d-b4fe-277fe7305bf02020-09-28Warnings, Adverse reactionsExact identifier
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLProficient Rx LP0003eccd-6147-4a7c-ae83-b2a94933e07d2020-08-01Warnings, Adverse reactionsExact identifier
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLGland Pharma Limited44c7fe99-8999-4747-9376-f13d3f9e56882020-07-18Warnings, Adverse reactionsExact identifier
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLMeitheal Pharmaceuticals Inc.b60000fc-e99b-4994-9d36-3907e0da9e062019-12-10Warnings, Adverse reactionsExact identifier
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLDr.Reddys Laboratories Inc.,c88898af-5cd8-7bed-a03e-2ab4488e20402018-11-30Warnings, Adverse reactionsExact identifier
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLAphena Pharma Solutions - Tennessee, LLCd825e4d6-8b00-473a-a6e6-90f5c3ad5bec2018-10-24Warnings, Adverse reactionsExact identifier
unii: 125OD7737X
MethocarbamolMETHOCARBAMOL TABLETSAphena Pharma Solutions - Tennessee, LLC3757cd8e-6054-4b75-bb04-d11f34c65cbe2018-09-12Warnings, Adverse reactionsExact identifier
unii: 125OD7737X

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.