Metoclopramide

Product NDC
0440-1771
11-digit product format
004401771
Labeler code
0440
Product ID
0440-1771_b120cbd9-1ea1-4972-ab81-7c1385c734f2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoclopramide
Dosage form
TABLET
Route
ORAL
Labeler
Liberty Pharmaceuticals, Inc.
Application
ANDA070184
Marketing category
ANDA
Marketing start
1990-09-30
Marketing end
0000-00-00
Substance
METOCLOPRAMIDE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [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
86441fd8-22b8-41db-bb26-c70dffc3923bProduct name120210111
340a6817-217a-4b71-9e83-8e2e60c4b0c5Product name120150319
1f2c49ec-0a44-8021-ecde-b27ece080b13Product name120140508
46471181-3fa6-5fcd-1d9f-1bb9d2b06171Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0440-1771-152020-01-31C16284748780-19d75b9d0-cdb4-f424-e053-dadaa90a57ceMETOCLOPRAMIDE TABLETS, USP 2204 2203

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0440-1771-15Metoclopramide15 in 1 BOTTLE, PLASTICTABLET152

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0440-1771-15EA - Each0440-1771c4baa928-0da7-4f78-a8a4-153c6498786b12013-10-17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
METOCLOPRAMIDE HYDROCHLORIDEACTIVE INGREDIENTW1792A2RVDMETOCLOPRAMIDE TABLET [LIBERTY PHARMACEUTICALS, INC.]2
METOCLOPRAMIDEACTIVE MOIETYL4YEB44I46METOCLOPRAMIDE TABLET [LIBERTY PHARMACEUTICALS, INC.]2
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUSINACTIVE INGREDIENTL11K75P92JMETOCLOPRAMIDE TABLET [LIBERTY PHARMACEUTICALS, INC.]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UMETOCLOPRAMIDE TABLET [LIBERTY PHARMACEUTICALS, INC.]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30METOCLOPRAMIDE TABLET [LIBERTY PHARMACEUTICALS, INC.]2
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2METOCLOPRAMIDE TABLET [LIBERTY PHARMACEUTICALS, INC.]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJMETOCLOPRAMIDE TABLET [LIBERTY PHARMACEUTICALS, INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0440-1771METOCLOPRAMIDE TABLET [LIBERTY PHARMACEUTICALS, INC.]2Legacy NDC, 1 package rows20140224_77446215-12f4-4f80-98a6-b36996886859.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311666metoclopramide HCl 10 MG Oral TabletPSN77446215-12f4-4f80-98a6-b369968868592
311666metoclopramide 10 MG Oral TabletSCD77446215-12f4-4f80-98a6-b369968868592
311666metoclopramide (as metoclopramide HCl) 10 MG Oral TabletSY77446215-12f4-4f80-98a6-b369968868592

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
0440-1771-150044017711515 in 1 BOTTLE, PLASTICHistorical