Famotidine

Product NDC
15127-370
11-digit product format
151270370
Labeler code
15127
Product ID
15127-370_14f9b3e4-d31d-4e20-a402-a2c84d11a3f1
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Select Brand
Application
ANDA090283
Marketing category
ANDA
Marketing start
2012-02-13
Marketing end
0000-00-00
Substance
FAMOTIDINE
Active strength
10 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
396bde5c-c78e-2f8b-ab1f-2ee6ba32bcaeProduct name720260317
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
cf645750-2e70-f6e1-c05a-a52847def5ddProduct name920250312
4fdc761c-585e-054b-8ebe-86130a26e4c1Product name220221205
fc2e1e31-353a-2c24-a4b4-fcf93bf7e38eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
15127-370-122020-01-31C16284748780-19d75b9d0-6acf-f424-e053-dadaa90a57ceDrug Facts
15127-370-302020-01-31C16284748780-19d75b9d0-6acf-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15127-370-12Famotidine1 in 1 CARTONTABLET, FILM COATED11
15127-370-12Famotidine12 in 1 BLISTER PACKTABLET, FILM COATED121
15127-370-30Famotidine30 in 1 BLISTER PACKTABLET, FILM COATED301
15127-370-30Famotidine1 in 1 CARTONTABLET, FILM COATED11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FAMOTIDINEACTIVE INGREDIENT5QZO15J2Z8FAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
FAMOTIDINEACTIVE MOIETY5QZO15J2Z8FAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UFAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
COLLOIDAL SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4FAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675FAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
HYDROXYPROPYL CELLULOSEINACTIVE INGREDIENTRFW2ET671PFAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOFAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30FAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQFAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
STARCH, PREGELATINIZED CORNINACTIVE INGREDIENTO8232NY3SJFAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
TALCINACTIVE INGREDIENT7SEV7J4R1UFAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPFAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15127-370FAMOTIDINE TABLET, FILM COATED [SELECT BRAND]1Legacy NDC, 4 package rows20130718_2a9153f1-3778-4f6f-b9b0-4c0bcaf49060.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199047famotidine 10 MG Oral TabletPSN2a9153f1-3778-4f6f-b9b0-4c0bcaf490601
199047famotidine 10 MG Oral TabletSCD2a9153f1-3778-4f6f-b9b0-4c0bcaf490601

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
15127-370-12151270370121 in 1 CARTONHistorical
15127-370-301512703703030 in 1 BLISTER PACKHistorical