FDA.reportPublic FDA data

Famotidine

Product NDC
67046-172
11-digit product format
670460172
Labeler code
67046
Product ID
67046-172_7d661e2c-6cce-35ab-e053-2a91aa0af61f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Contract Pharmacy Services-PA
Application
ANDA075511
Marketing category
ANDA
Marketing start
2017-09-20
Marketing end
0000-00-00
Substance
FAMOTIDINE
Active strength
20 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
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
67046-172-072020-01-31C16284748780-19d75b9cf-e8fa-f424-e053-dadaa90a57ceFamotidine Tablets USP 172 5728 5729 Rx only
67046-172-142020-01-31C16284748780-19d75b9cf-e8fa-f424-e053-dadaa90a57ceFamotidine Tablets USP 172 5728 5729 Rx only
67046-172-152020-01-31C16284748780-19d75b9cf-e8fa-f424-e053-dadaa90a57ceFamotidine Tablets USP 172 5728 5729 Rx only
67046-172-202020-01-31C16284748780-19d75b9cf-e8fa-f424-e053-dadaa90a57ceFamotidine Tablets USP 172 5728 5729 Rx only
67046-172-212020-01-31C16284748780-19d75b9cf-e8fa-f424-e053-dadaa90a57ceFamotidine Tablets USP 172 5728 5729 Rx only
67046-172-282020-01-31C16284748780-19d75b9cf-e8fa-f424-e053-dadaa90a57ceFamotidine Tablets USP 172 5728 5729 Rx only
67046-172-302020-01-31C16284748780-19d75b9cf-e8fa-f424-e053-dadaa90a57ceFamotidine Tablets USP 172 5728 5729 Rx only
67046-172-602020-01-31C16284748780-19d75b9cf-e8fa-f424-e053-dadaa90a57ceFamotidine Tablets USP 172 5728 5729 Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67046-172-07Famotidine7 in 1 BLISTER PACKTABLET, FILM COATED72
67046-172-14Famotidine14 in 1 BLISTER PACKTABLET, FILM COATED142
67046-172-15Famotidine15 in 1 BLISTER PACKTABLET, FILM COATED152
67046-172-20Famotidine20 in 1 BLISTER PACKTABLET, FILM COATED202
67046-172-21Famotidine21 in 1 BLISTER PACKTABLET, FILM COATED212
67046-172-28Famotidine28 in 1 BLISTER PACKTABLET, FILM COATED282
67046-172-30Famotidine30 in 1 BLISTER PACKTABLET, FILM COATED302
67046-172-60Famotidine60 in 1 BLISTER PACKTABLET, FILM COATED602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67046-172FAMOTIDINE TABLET, FILM COATED [CONTRACT PHARMACY SERVICES-PA]2Legacy NDC, 8 package rows20181220_599f4348-122c-adc9-e053-2a91aa0acd21.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310273famotidine 20 MG Oral TabletPSN599f4348-122c-adc9-e053-2a91aa0acd212
310273famotidine 20 MG Oral TabletSCD599f4348-122c-adc9-e053-2a91aa0acd212

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
67046-172-07670460172077 in 1 BLISTER PACKHistorical
67046-172-146704601721414 in 1 BLISTER PACKHistorical
67046-172-156704601721515 in 1 BLISTER PACKHistorical
67046-172-206704601722020 in 1 BLISTER PACKHistorical
67046-172-216704601722121 in 1 BLISTER PACKHistorical
67046-172-286704601722828 in 1 BLISTER PACKHistorical
67046-172-306704601723030 in 1 BLISTER PACKHistorical
67046-172-606704601726060 in 1 BLISTER PACKHistorical