Methocarbamol

Product NDC
72789-041
11-digit product format
727890041
Labeler code
72789
Product ID
72789-041_4af347a6-c3c7-7d45-e063-6294a90a1132
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
72789-041-20Methocarbamol20 in 1 BOTTLE, PLASTICTABLET, FILM COATED2015
72789-041-30Methocarbamol30 in 1 BOTTLE, PLASTICTABLET, FILM COATED3015
72789-041-40Methocarbamol40 in 1 BOTTLE, PLASTICTABLET, FILM COATED4015
72789-041-60Methocarbamol60 in 1 BOTTLE, PLASTICTABLET, FILM COATED6015

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72789-041-20EA - Each72789-041eb0728b4-92e8-4239-ada4-b9ed9eecb4a912020-04-20
72789-041-30EA - Each72789-0417f8390b3-9dab-4b7e-9e29-f799b095e40612020-02-13
72789-041-40EA - Each72789-04174265b1b-23c7-4677-8499-554e99e3937d12020-02-13
72789-041-60EA - Each72789-04164bd5fb6-19af-4270-b7ec-7b9960f3a5a212020-02-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72789-041METHOCARBAMOL TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13Current NDC, Legacy NDC, 4 package rows20240522_440bf1ba-a704-4c35-bece-0a0987fc0c11.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197944methocarbamol 750 MG Oral TabletPSN440bf1ba-a704-4c35-bece-0a0987fc0c1115
197944methocarbamol 750 MG Oral TabletSCD440bf1ba-a704-4c35-bece-0a0987fc0c1115

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
72789-041-207278900412020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20) 2020-02-130000-00-00NoNoCurrent
72789-041-307278900413030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30) 2020-01-160000-00-00NoNoCurrent
72789-041-407278900414040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40) 2020-01-060000-00-00NoNoCurrent
72789-041-607278900416060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60) 2019-12-190000-00-00NoNoCurrent