Famotidine

Product NDC
37808-036
11-digit product format
378080036
Labeler code
37808
Product ID
37808-036_f16a5de0-aad1-474d-8fe0-e396627aa0b0
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
HEB
Application
ANDA090283
Marketing category
ANDA
Marketing start
2014-04-09
Marketing end
0000-00-00
Substance
FAMOTIDINE
Active strength
20 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
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
37808-036-262021-01-29C16284748780-1ba0f9c33-1033-a910-e053-dadaa90a0b85Drug Facts
37808-036-502021-01-29C16284748780-1ba0f9c33-1033-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-036-26Famotidine1 in 1 CARTONTABLET, FILM COATED13
37808-036-26Famotidine25 in 1 BOTTLETABLET, FILM COATED253
37808-036-50Famotidine50 in 1 BOTTLETABLET, FILM COATED503
37808-036-50Famotidine1 in 1 CARTONTABLET, FILM COATED13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FAMOTIDINEACTIVE INGREDIENT5QZO15J2Z8FAMOTIDINE TABLET, FILM COATED [HEB]1
FAMOTIDINEACTIVE MOIETY5QZO15J2Z8FAMOTIDINE TABLET, FILM COATED [HEB]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UFAMOTIDINE TABLET, FILM COATED [HEB]1
HYDROXYPROPYL CELLULOSE (TYPE H)INACTIVE INGREDIENTRFW2ET671PFAMOTIDINE TABLET, FILM COATED [HEB]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOFAMOTIDINE TABLET, FILM COATED [HEB]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30FAMOTIDINE TABLET, FILM COATED [HEB]1
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AFAMOTIDINE TABLET, FILM COATED [HEB]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4FAMOTIDINE TABLET, FILM COATED [HEB]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJFAMOTIDINE TABLET, FILM COATED [HEB]1
TALCINACTIVE INGREDIENT7SEV7J4R1UFAMOTIDINE TABLET, FILM COATED [HEB]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPFAMOTIDINE TABLET, FILM COATED [HEB]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-036FAMOTIDINE TABLET, FILM COATED [HEB]3Legacy NDC, 4 package rows20190213_4c077059-3074-4cd9-88e8-aef26af82953.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310273famotidine 20 MG Oral TabletPSN4c077059-3074-4cd9-88e8-aef26af829533
310273famotidine 20 MG Oral TabletSCD4c077059-3074-4cd9-88e8-aef26af829533

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
37808-036-26378080036261 in 1 CARTONHistorical
37808-036-503780800365050 in 1 BOTTLEHistorical