FDA.reportPublic FDA data

Methocarbamol

Product NDC
72189-665
11-digit product format
721890665
Labeler code
72189
Product ID
72189-665_4ddb0161-0d2f-98db-e063-6294a90a8704
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Direct_rx
Application
ANDA040489
Marketing category
ANDA
Marketing start
2026-03-06
Substance
METHOCARBAMOL
Active strength
500 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Methocarbamol
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METHOCARBAMOL500 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii125OD7737X
Rxcui197943

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
492965be-47bc-38cf-57c4-5c5e0343abe5Product name620211028
02a01e9c-3f4e-c0ee-6542-be865127aea3Product name820190205

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72189-665-30Methocarbamol30 in 1 BOTTLETABLET302
72189-665-60Methocarbamol60 in 1 BOTTLETABLET602

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197943methocarbamol 500 MG Oral TabletPSN4c5c8933-a4b5-f9c2-e063-6294a90a6f002
197943methocarbamol 500 MG Oral TabletSCD4c5c8933-a4b5-f9c2-e063-6294a90a6f002

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72189-665-307218906653030 TABLET in 1 BOTTLE (72189-665-30) 30 tablet2026-03-06NoNoCurrent
72189-665-607218906656060 TABLET in 1 BOTTLE (72189-665-60) 60 tablet2026-03-06NoNoCurrent