Famotidine

Product NDC
37012-036
11-digit product format
370120036
Labeler code
37012
Product ID
37012-036_1ab4ceb0-cbc8-414a-a843-e81625122e0c
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Shopko Stores Operating Co., LLC
Application
ANDA090283
Marketing category
ANDA
Marketing start
2010-07-23
Marketing end
0000-00-00
Substance
FAMOTIDINE
Active strength
20 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
37012-036-262020-01-31C16284748780-19d75b9d0-5c3b-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37012-036-26Famotidine25 in 1 BOTTLETABLET, FILM COATED251

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37012-036FAMOTIDINE TABLET, FILM COATED [SHOPKO STORES OPERATING CO., LLC]1Legacy NDC, 1 package rows20130323_f7a7a24b-ecd9-4dab-9d1e-0b03aa99c08e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310273famotidine 20 MG Oral TabletPSNf7a7a24b-ecd9-4dab-9d1e-0b03aa99c08e1
310273famotidine 20 MG Oral TabletSCDf7a7a24b-ecd9-4dab-9d1e-0b03aa99c08e1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
37012-036-263701200362625 in 1 BOTTLEHistorical