FDA.reportPublic FDA data

Methocarbamol

Product NDC
71205-103
11-digit product format
712050103
Labeler code
71205
Product ID
71205-103_185894ce-3da6-4a5b-83e6-daeba7b3c362
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methocarbamol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA208507
Marketing category
ANDA
Marketing start
2018-01-15
Substance
METHOCARBAMOL
Active strength
500 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
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
71205-103-20Methocarbamol20 in 1 BOTTLETABLET, FILM COATED204
71205-103-30Methocarbamol30 in 1 BOTTLETABLET, FILM COATED304
71205-103-40Methocarbamol40 in 1 BOTTLETABLET, FILM COATED404
71205-103-45Methocarbamol45 in 1 BOTTLETABLET, FILM COATED454
71205-103-60Methocarbamol60 in 1 BOTTLETABLET, FILM COATED604
71205-103-90Methocarbamol90 in 1 BOTTLETABLET, FILM COATED904

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-103-20EA - Each71205-10345f7e188-f3a5-4d72-bc9f-baab3b6caa1b12018-11-06
71205-103-90EA - Each71205-10307c58f11-fe0e-4601-b438-76fe3125c3ea12018-12-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-103METHOCARBAMOL TABLET, FILM COATED [PROFICIENT RX LP]4Current NDC, Legacy NDC, 6 package rows20210501_39b4362e-a26e-49cb-9d06-898bc9b0e005.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197943methocarbamol 500 MG Oral TabletPSN39b4362e-a26e-49cb-9d06-898bc9b0e0054
197943methocarbamol 500 MG Oral TabletSCD39b4362e-a26e-49cb-9d06-898bc9b0e0054

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71205-103-207120501032020 TABLET, FILM COATED in 1 BOTTLE (71205-103-20) 2018-09-040000-00-00NoNoCurrent
71205-103-307120501033030 TABLET, FILM COATED in 1 BOTTLE (71205-103-30) 2018-09-040000-00-00NoNoCurrent
71205-103-407120501034040 TABLET, FILM COATED in 1 BOTTLE (71205-103-40) 2018-09-040000-00-00NoNoCurrent
71205-103-457120501034545 TABLET, FILM COATED in 1 BOTTLE (71205-103-45) 2018-09-040000-00-00NoNoCurrent
71205-103-607120501036060 TABLET, FILM COATED in 1 BOTTLE (71205-103-60) 2018-09-040000-00-00NoNoCurrent
71205-103-907120501039090 TABLET, FILM COATED in 1 BOTTLE (71205-103-90) 2018-09-040000-00-00NoNoCurrent