Methocarbamol

Product NDC
80425-0283
11-digit product format
804250283
Labeler code
80425
Product ID
80425-0283_2a9ba8f4-6ceb-e827-e063-6394a90a0300
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA040489
Marketing category
ANDA
Marketing start
2023-03-07
Substance
METHOCARBAMOL
Active strength
500 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
125OD7737XMETHOCARBAMOL532-03-6METHOCARBAMOL

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80425-0283-18042502830130 TABLET in 1 BOTTLE (80425-0283-1) 30 tablet2023-03-07NoNoHistorical
80425-0283-28042502830260 TABLET in 1 BOTTLE (80425-0283-2) 60 tablet2023-03-07NoNoHistorical
80425-0283-38042502830390 TABLET in 1 BOTTLE (80425-0283-3) 90 tablet2023-03-07NoNoHistorical
80425-0283-480425028304120 TABLET in 1 BOTTLE (80425-0283-4) 120 tablet2023-03-07NoNoHistorical
80425-0283-580425028305180 TABLET in 1 BOTTLE (80425-0283-5) 180 tablet2023-03-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Methocarbamol TabletsAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL3