METHOCARBAMOL

Product NDC
72189-284
11-digit product format
721890284
Labeler code
72189
Product ID
72189-284_2c293420-98b4-a209-e063-6394a90a5797
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METHOCARBAMOL
Dosage form
TABLET
Route
ORAL
Labeler
DirectRx
Application
ANDA040489
Marketing category
ANDA
Marketing start
2021-10-19
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
72189-284-307218902843030 TABLET in 1 BOTTLE (72189-284-30) 30 tablet2021-10-19NoNoHistorical
72189-284-607218902846060 TABLET in 1 BOTTLE (72189-284-60) 60 tablet2021-10-19NoNoHistorical
72189-284-7272189028472120 TABLET in 1 BOTTLE (72189-284-72) 120 tablet2021-10-19NoNoHistorical
72189-284-907218902849090 TABLET in 1 BOTTLE (72189-284-90) 90 tablet2021-10-19NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
MethocarbamolDirectRx2025-01-20HUMAN PRESCRIPTION DRUG LABEL5