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 2 of 9 · 171 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MethocarbamolMETHOCARBAMOLA-S Medication Solutionscfdc0d68-00ad-44d6-b932-819cc3d5d60e2026-06-26Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLA-S Medication Solutionsb81a8e64-ae41-409b-94a6-b36cb50bc25d2026-06-26Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLHAWAII REPACK, INC.c4744824-4c74-411d-aa8e-c63ee9d899132026-06-25Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOL TABLETSPreferred Pharmaceuticals Inc.43f83b87-e169-46fe-98bd-6af373595bd32026-06-23Warnings, Adverse reactionsExact identifier
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLPreferred Pharmaceuticals Inc.4ef1c2c0-31e1-4f85-b645-ff47a057a9942026-06-23Warnings, Adverse reactionsExact identifier
application number: ANDA040489
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLPreferred Pharmaceuticals, Inc425abc3b-2111-4fac-bf27-b685d1e657af2026-06-23Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOL TABLETSPreferred Pharmaceuticals Inc.e03878d3-d780-4e7f-b828-20ac2a1099332026-06-23Warnings, Adverse reactionsExact identifier
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLDirect_rx4c5c8933-a4b5-f9c2-e063-6294a90a6f002026-06-16Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLBryant Ranch Prepack5af36a83-2b36-4fe2-8c6a-61b5516214212026-06-16Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLBryant Ranch Prepackcc004f5c-d5fc-48c5-9f37-c59b9c37e1132026-06-16Warnings, Adverse reactionsExact identifier
application number: ANDA040489
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLBryant Ranch Prepack9076b4ad-17be-4933-a975-7bf80cc92b492026-06-10Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLBryant Ranch Prepack3f8aed5d-ba8d-4c32-872b-08ab15240cc12026-06-10Warnings, Adverse reactionsExact identifier
application number: ANDA040489
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLCardinal Health 107, LLC50603730-9f69-4ed7-bccf-31c474f83e142026-06-05Warnings, Adverse reactionsExact identifier
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLSt. Mary's Medical Park Pharmacyfd8cac57-9664-1fa0-e053-6294a90af8722026-06-02Warnings, Adverse reactionsExact identifier
application number: ANDA040489
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLBryant Ranch Prepack6466438c-4609-4554-8919-35710a1b556d2026-06-01Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLBryant Ranch Prepack3212f121-9428-4186-8f00-accf08bca4732026-05-29Warnings, Adverse reactionsExact identifier
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLBryant Ranch Prepack33f89a57-f65d-4e99-a3a3-690ef805d8692026-05-27Warnings, Adverse reactionsExact identifier
application number: ANDA040489
unii: 125OD7737X
MethocarbamolMETHOCARBAMOLBryant Ranch Prepack6af87b4e-6507-4190-b043-a6d3b440314a2026-05-27Warnings, Adverse reactionsExact identifier
application number: ANDA040489
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOL TABLETSCoupler LLC52b87514-e6e0-ab57-e063-6394a90a6b232026-05-26Warnings, Adverse reactionsExact identifier
rxcui: 197943
unii: 125OD7737X
MethocarbamolMETHOCARBAMOL TABLETSNuCare Pharmaceuticals,Inc.71c21226-cd96-33ed-e053-2995a90a52692026-05-22Warnings, Adverse reactionsExact identifier
unii: 125OD7737X

Reported adverse events (FAERS/openFDA)#

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