Methocarbamol

Product NDC
10544-956
11-digit product format
105440956
Labeler code
10544
Product ID
10544-956_5eb54c7b-2566-4570-95db-b39bfaf47d64
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Blenheim Pharmacal, Inc.
Application
ANDA040489
Marketing category
ANDA
Marketing start
2016-01-07
Marketing end
0000-00-00
Substance
METHOCARBAMOL
Active strength
750 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
492965be-47bc-38cf-57c4-5c5e0343abe5Product name620211028
02a01e9c-3f4e-c0ee-6542-be865127aea3Product name820190205

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10544-956-30Methocarbamol30 in 1 BOTTLE, PLASTICTABLET301
10544-956-60Methocarbamol60 in 1 BOTTLE, PLASTICTABLET601
10544-956-90Methocarbamol90 in 1 BOTTLE, PLASTICTABLET901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10544-956METHOCARBAMOL TABLET [BLENHEIM PHARMACAL, INC.]1Legacy NDC, 3 package rows20160108_6cd12362-bdaa-43ca-9089-c02b17692de9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197944methocarbamol 750 MG Oral TabletPSN6cd12362-bdaa-43ca-9089-c02b17692de91
197944methocarbamol 750 MG Oral TabletSCD6cd12362-bdaa-43ca-9089-c02b17692de91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
10544-956-301054409563030 in 1 BOTTLE, PLASTICHistorical
10544-956-601054409566060 in 1 BOTTLE, PLASTICHistorical
10544-956-901054409569090 in 1 BOTTLE, PLASTICHistorical