Methocarbamol

Product NDC
0440-1740
11-digit product format
004401740
Labeler code
0440
Product ID
0440-1740_818d8de8-3e05-4714-882a-f68f6fc6e563
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methocarbamol
Dosage form
TABLET
Route
ORAL
Labeler
Liberty Pharmaceuticals, Inc.
Application
ANDA040489
Marketing category
ANDA
Marketing start
2003-01-29
Marketing end
0000-00-00
Substance
METHOCARBAMOL
Active strength
500 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC exclude flag
E
Listing certified through
2018-12-31
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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0440-1740-402020-01-31C16284748780-19d75b9d0-2b3c-f424-e053-dadaa90a57ceMethocarbamol Tablets, USP 500 mg Methocarbamol Tablets, USP 750 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0440-1740-40Methocarbamol40 in 1 BOTTLE, PLASTICTABLET401

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0440-1740-40EA - Each0440-1740a62675f7-5465-42f7-a416-d5b76c18889012013-10-17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
METHOCARBAMOLACTIVE INGREDIENT125OD7737XMETHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1
METHOCARBAMOLACTIVE MOIETY125OD7737XMETHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30METHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1
POVIDONESINACTIVE INGREDIENTFZ989GH94EMETHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4METHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2METHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJMETHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APMETHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RMETHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0440-1740METHOCARBAMOL TABLET [LIBERTY PHARMACEUTICALS, INC.]1Legacy NDC, 1 package rows20130906_bfef8c57-1044-4723-b1bc-ce15fbbce6c3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197943methocarbamol 500 MG Oral TabletPSNbfef8c57-1044-4723-b1bc-ce15fbbce6c31
197943methocarbamol 500 MG Oral TabletSCDbfef8c57-1044-4723-b1bc-ce15fbbce6c31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
0440-1740-400044017404040 in 1 BOTTLE, PLASTICHistorical