FDA.reportPublic FDA data

Methocarbamol

Product NDC
71335-1727
11-digit product format
713351727
Labeler code
71335
Product ID
71335-1727_fc9c7b08-e298-aa25-e053-6294a90aca75
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA086988
Marketing category
ANDA
Marketing start
2013-01-15
Substance
METHOCARBAMOL
Active strength
750 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Methocarbamol
Listing expiration
2026-12-31

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
71335-1727-0Methocarbamol14 in 1 BOTTLETABLET14103
71335-1727-1Methocarbamol20 in 1 BOTTLETABLET20103
71335-1727-2Methocarbamol30 in 1 BOTTLETABLET30103
71335-1727-3Methocarbamol40 in 1 BOTTLETABLET40103
71335-1727-4Methocarbamol120 in 1 BOTTLETABLET120103
71335-1727-5Methocarbamol60 in 1 BOTTLETABLET60103
71335-1727-6Methocarbamol90 in 1 BOTTLETABLET90103
71335-1727-7Methocarbamol112 in 1 BOTTLETABLET112103
71335-1727-8Methocarbamol21 in 1 BOTTLETABLET21103
71335-1727-9Methocarbamol84 in 1 BOTTLETABLET84103

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-1727-1EA - Each71335-17272385a2dc-5f7f-4839-86cb-f7b2cb88477612021-09-07
71335-1727-2EA - Each71335-1727eb640200-4c1a-4b12-88a4-a64f830fa1d412021-09-07
71335-1727-3EA - Each71335-1727f14ca18b-b4ed-42a0-893b-2570bcb16a8a12021-09-07
71335-1727-4EA - Each71335-1727814ad5c6-a15c-4e00-90e5-38667e62b6cd12021-09-07
71335-1727-5EA - Each71335-1727c65cda95-2942-4ef9-8a8c-4316965187a512021-09-07
71335-1727-6EA - Each71335-172771fc180b-2dbc-456d-9b8c-c4ecc609859612021-09-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1727METHOCARBAMOL TABLET [BRYANT RANCH PREPACK]103Current NDC, Legacy NDC, 10 package rows20230603_4003026f-ed9e-40ac-9e7e-5e28d32d7cb8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197944methocarbamol 750 MG Oral TabletPSN4003026f-ed9e-40ac-9e7e-5e28d32d7cb8103
197944methocarbamol 750 MG Oral TabletSCD4003026f-ed9e-40ac-9e7e-5e28d32d7cb8103

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1727-07133517270014 TABLET in 1 BOTTLE (71335-1727-0) 14 tablet2021-12-290000-00-00NoNoCurrent
71335-1727-17133517270120 TABLET in 1 BOTTLE (71335-1727-1) 20 tablet2021-04-220000-00-00NoNoCurrent
71335-1727-27133517270230 TABLET in 1 BOTTLE (71335-1727-2) 30 tablet2020-11-050000-00-00NoNoCurrent
71335-1727-37133517270340 TABLET in 1 BOTTLE (71335-1727-3) 40 tablet2021-02-160000-00-00NoNoCurrent
71335-1727-471335172704120 TABLET in 1 BOTTLE (71335-1727-4) 120 tablet2021-04-010000-00-00NoNoCurrent
71335-1727-57133517270560 TABLET in 1 BOTTLE (71335-1727-5) 60 tablet2021-01-080000-00-00NoNoCurrent
71335-1727-67133517270690 TABLET in 1 BOTTLE (71335-1727-6) 90 tablet2020-11-040000-00-00NoNoCurrent
71335-1727-771335172707112 TABLET in 1 BOTTLE (71335-1727-7) 112 tablet2021-12-290000-00-00NoNoCurrent
71335-1727-87133517270821 TABLET in 1 BOTTLE (71335-1727-8) 21 tablet2021-12-290000-00-00NoNoCurrent
71335-1727-97133517270984 TABLET in 1 BOTTLE (71335-1727-9) 84 tablet2021-12-290000-00-00NoNoCurrent