FDA.reportPublic FDA data

Methocarbamol

Product NDC
82804-273
11-digit product format
828040273
Labeler code
82804
Product ID
82804-273_311c79a5-1447-4fef-8726-ae003ef64db5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA040489
Marketing category
ANDA
Marketing start
2025-05-22
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
82804-273-30Methocarbamol30 in 1 BOTTLETABLET301
82804-273-90Methocarbamol90 in 1 BOTTLETABLET901

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197943methocarbamol 500 MG Oral TabletPSN311c79a5-1447-4fef-8726-ae003ef64db51
197943methocarbamol 500 MG Oral TabletSCD311c79a5-1447-4fef-8726-ae003ef64db51

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82804-273-308280402733030 TABLET in 1 BOTTLE (82804-273-30) 30 tablet2026-03-13NoNoCurrent
82804-273-908280402739090 TABLET in 1 BOTTLE (82804-273-90) 90 tablet2026-03-13NoNoCurrent