Equaline

Product NDC
41163-351
11-digit product format
411630351
Labeler code
41163
Product ID
41163-351_b15d3c38-c3b9-4830-9e4e-7eee66b3b782
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine
Dosage form
TABLET
Route
ORAL
Labeler
Supervalu Inc.
Application
ANDA200536
Marketing category
ANDA
Marketing start
2011-06-28
Marketing end
0000-00-00
Substance
RANITIDINE HYDROCHLORIDE
Active strength
150 mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7f54af34-be54-4c3c-894f-78df6452d747Product name320190703
ccf8541e-b7dc-e6ba-06c9-15bf143a7850Product name520190611
05700d9e-ea6f-4aab-b0ed-1488f1d85d7bProduct name120180904
2f9d4e5c-e179-490e-8c43-f19e1e0ca228Product name120160720

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41163-351-242020-01-31C16284748780-19d75b9d0-024a-f424-e053-dadaa90a57ceDrug Facts
41163-351-502020-01-31C16284748780-19d75b9d0-024a-f424-e053-dadaa90a57ceDrug Facts
41163-351-652020-01-31C16284748780-19d75b9d0-024a-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41163-351-24Equaline1 in 1 BLISTER PACKTABLET11
41163-351-24Equaline24 in 1 CARTONTABLET241
41163-351-50Equaline1 in 1 CARTONTABLET11
41163-351-50Equaline50 in 1 BOTTLETABLET501
41163-351-65Equaline1 in 1 CARTONTABLET11
41163-351-65Equaline65 in 1 BOTTLETABLET651

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
41163-351-24EA - Each41163-35114e9bcef-5647-45c5-bb7d-38a50e0cb8b712016-12-07
41163-351-50EA - Each41163-351c3a697e6-720f-4211-847e-f9d721ce53f112016-12-07

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
RANITIDINE HYDROCHLORIDEACTIVE INGREDIENTBK76465IHMEQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
RANITIDINEACTIVE MOIETY884KT10YB7EQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UEQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48EQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675EQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOEQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30EQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AEQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4EQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
TALCINACTIVE INGREDIENT7SEV7J4R1UEQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPEQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41163-351EQUALINE (RANITIDINE) TABLET [SUPERVALU INC.]1Legacy NDC, 6 package rows20150403_b15d3c38-c3b9-4830-9e4e-7eee66b3b782.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198191ranitidine 150 MG Oral TabletPSNb15d3c38-c3b9-4830-9e4e-7eee66b3b7821
198191ranitidine 150 MG Oral TabletSCDb15d3c38-c3b9-4830-9e4e-7eee66b3b7821
198191ranitidine 150 MG (as ranitidine HCl 168 MG) Oral TabletSYb15d3c38-c3b9-4830-9e4e-7eee66b3b7821

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
41163-351-24411630351241 in 1 BLISTER PACKHistorical
41163-351-50411630351501 in 1 CARTONHistorical
41163-351-65411630351651 in 1 CARTONHistorical