Methocarbamol

Product NDC
71205-285
11-digit product format
712050285
Labeler code
71205
Product ID
71205-285_16891834-bb2f-48b9-9dc4-89ab7c34f1f8
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
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
71205-285-30Methocarbamol30 in 1 BOTTLETABLET, FILM COATED304
71205-285-40Methocarbamol40 in 1 BOTTLETABLET, FILM COATED404
71205-285-45Methocarbamol45 in 1 BOTTLETABLET, FILM COATED454
71205-285-60Methocarbamol60 in 1 BOTTLETABLET, FILM COATED604
71205-285-90Methocarbamol90 in 1 BOTTLETABLET, FILM COATED904

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-285-30EA - Each71205-285737fdbf1-8b5b-483a-90a8-385c4da767df12020-01-03
71205-285-40EA - Each71205-285be1e690c-6218-41df-9f86-9cfc456223e512020-02-13
71205-285-45EA - Each71205-28599498f85-b4d3-4ac3-b7cb-819022a6be5a12019-08-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-285METHOCARBAMOL TABLET, FILM COATED [PROFICIENT RX LP]4Current NDC, Legacy NDC, 5 package rows20220421_201205d1-22f2-46bb-b298-02d4978ba568.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197944methocarbamol 750 MG Oral TabletPSN201205d1-22f2-46bb-b298-02d4978ba5684
197944methocarbamol 750 MG Oral TabletSCD201205d1-22f2-46bb-b298-02d4978ba5684

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71205-285-307120502853030 TABLET, FILM COATED in 1 BOTTLE (71205-285-30) 2019-06-010000-00-00NoNoCurrent
71205-285-407120502854040 TABLET, FILM COATED in 1 BOTTLE (71205-285-40) 2019-11-010000-00-00NoNoCurrent
71205-285-457120502854545 TABLET, FILM COATED in 1 BOTTLE (71205-285-45) 2019-06-010000-00-00NoNoCurrent
71205-285-607120502856060 TABLET, FILM COATED in 1 BOTTLE (71205-285-60) 2019-06-010000-00-00NoNoCurrent
71205-285-907120502859090 TABLET, FILM COATED in 1 BOTTLE (71205-285-90) 2019-06-010000-00-00NoNoCurrent