Methocarbamol

Product NDC
72789-022
11-digit product format
727890022
Labeler code
72789
Product ID
72789-022_4af2ff79-e0d9-6484-e063-6394a90ad124
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA208507
Marketing category
ANDA
Marketing start
2018-01-15
Substance
METHOCARBAMOL
Active strength
750 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
METHOCARBAMOL750 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii125OD7737X
Rxcui197944

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
72789-022-01Methocarbamol100 in 1 BOTTLE, PLASTICTABLET, FILM COATED10014
72789-022-82Methocarbamol500 in 1 BOTTLE, PLASTICTABLET, FILM COATED50014
72789-022-90Methocarbamol90 in 1 BOTTLE, PLASTICTABLET, FILM COATED9014
72789-022-93Methocarbamol180 in 1 BOTTLE, PLASTICTABLET, FILM COATED18014
72789-022-98Methocarbamol120 in 1 BOTTLE, PLASTICTABLET, FILM COATED12014

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72789-022-01EA - Each72789-022bbdb976e-ebcb-49dc-9040-1003d75399e512019-11-12
72789-022-82EA - Each72789-022f61cb066-7222-419e-ad80-2304961d296412019-11-12
72789-022-90EA - Each72789-02201071f32-7ba3-47cb-8097-53bacd1389f112023-10-16
72789-022-93EA - Each72789-022e2caeab1-3249-430c-b8f0-c9e43e7df56012023-10-16
72789-022-98EA - Each72789-0222e728c26-e3d4-4730-8340-b7006169c52812023-10-16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72789-022METHOCARBAMOL TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]12Current NDC, Legacy NDC, 5 package rows20240417_3b0e60a7-3cff-4665-a473-ad3257619cdd.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197944methocarbamol 750 MG Oral TabletPSN3b0e60a7-3cff-4665-a473-ad3257619cdd14
197944methocarbamol 750 MG Oral TabletSCD3b0e60a7-3cff-4665-a473-ad3257619cdd14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
72789-022-0172789002201100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-01) 2019-10-240000-00-00NoNoCurrent
72789-022-8272789002282500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-82) 2019-10-240000-00-00NoNoCurrent
72789-022-907278900229090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-90) 2023-09-12NoNoCurrent
72789-022-9372789002293180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-93) 2023-09-12NoNoCurrent
72789-022-9872789002298120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-98) 2023-09-12NoNoCurrent