Ranitidine

Product NDC
0363-0352
11-digit product format
003630352
Labeler code
0363
Product ID
0363-0352_94d81b3b-2e78-4691-8bb0-f003fddc5395
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Walgreen Company
Application
ANDA201745
Marketing category
ANDA
Marketing start
2013-09-24
Marketing end
0000-00-00
Substance
RANITIDINE HYDROCHLORIDE
Active strength
75 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
0363-0352-082020-01-31C16284748780-19d75b9d0-061f-f424-e053-dadaa90a57ce9a0718f6-868c-4cf3-aacc-fe08a4d8754c
0363-0352-302020-01-31C16284748780-19d75b9d0-061f-f424-e053-dadaa90a57ce9a0718f6-868c-4cf3-aacc-fe08a4d8754c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0352-08Ranitidine80 in 1 BOTTLETABLET, FILM COATED801
0363-0352-08Ranitidine1 in 1 CARTONTABLET, FILM COATED11
0363-0352-30Ranitidine30 in 1 BOTTLETABLET, FILM COATED301
0363-0352-30Ranitidine1 in 1 CARTONTABLET, FILM COATED11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
RANITIDINE HYDROCHLORIDEACTIVE INGREDIENTBK76465IHMRANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
RANITIDINEACTIVE MOIETY884KT10YB7RANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61URANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48RANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675RANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WORANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30RANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQRANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4RANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
TALCINACTIVE INGREDIENT7SEV7J4R1URANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPRANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0352RANITIDINE TABLET, FILM COATED [WALGREEN COMPANY]1Legacy NDC, 4 package rows20131101_9a0718f6-868c-4cf3-aacc-fe08a4d8754c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312773ranitidine 75 MG Oral TabletPSN9a0718f6-868c-4cf3-aacc-fe08a4d8754c1
312773ranitidine 75 MG Oral TabletSCD9a0718f6-868c-4cf3-aacc-fe08a4d8754c1
312773ranitidine 75 MG (as ranitidine hydrochloride 84 MG) Oral TabletSY9a0718f6-868c-4cf3-aacc-fe08a4d8754c1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
0363-0352-080036303520880 in 1 BOTTLEHistorical
0363-0352-300036303523030 in 1 BOTTLEHistorical