Methocarbamol

Product NDC
80425-0275
11-digit product format
804250275
Labeler code
80425
Product ID
80425-0275_2a9b792b-f419-e859-e063-6394a90a30e2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA090200
Marketing category
ANDA
Marketing start
2023-02-17
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
80425-0275-18042502750130 TABLET in 1 BOTTLE (80425-0275-1) 30 tablet2023-02-17NoNoHistorical
80425-0275-28042502750260 TABLET in 1 BOTTLE (80425-0275-2) 60 tablet2023-02-17NoNoHistorical
80425-0275-38042502750390 TABLET in 1 BOTTLE (80425-0275-3) 90 tablet2023-02-17NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Methocarbamol TabletsAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL2