Ranitidine

Product NDC
37012-351
11-digit product format
370120351
Labeler code
37012
Product ID
37012-351_5e4f79dd-4223-4bb2-9335-b195fc32eed6
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine
Dosage form
TABLET
Route
ORAL
Labeler
Shopko Stores Operating Co., LLC
Application
ANDA200536
Marketing category
ANDA
Marketing start
2012-03-30
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
37012-351-502020-01-31C16284748780-19d75b9d0-2f41-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37012-351-50Ranitidine50 in 1 BOTTLETABLET501

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
RANITIDINE HYDROCHLORIDEACTIVE INGREDIENTBK76465IHMRANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
RANITIDINEACTIVE MOIETY884KT10YB7RANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61URANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
COLLOIDAL SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4RANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48RANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675RANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WORANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30RANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1ARANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
TALCINACTIVE INGREDIENT7SEV7J4R1URANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPRANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37012-351RANITIDINE TABLET [SHOPKO STORES OPERATING CO., LLC]1Legacy NDC, 1 package rows20130323_d352a511-6ee7-4d9a-a3e5-4b35ae6551b4.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198191ranitidine 150 MG Oral TabletPSNd352a511-6ee7-4d9a-a3e5-4b35ae6551b41
198191ranitidine 150 MG Oral TabletSCDd352a511-6ee7-4d9a-a3e5-4b35ae6551b41
198191ranitidine 150 MG (as ranitidine HCl 168 MG) Oral TabletSYd352a511-6ee7-4d9a-a3e5-4b35ae6551b41

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
37012-351-503701203515050 in 1 BOTTLEHistorical