Famotidine

Product NDC
60760-736
11-digit product format
607600736
Labeler code
60760
Product ID
60760-736_f4e949c2-910e-18be-e053-2995a90aec97
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Application
ANDA216441
Marketing category
ANDA
Marketing start
2022-12-08
Substance
FAMOTIDINE
Active strength
40 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Famotidine
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FAMOTIDINE40 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5QZO15J2Z8
Rxcui284245

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60760-736-07Famotidine7 in 1 BOTTLE, PLASTICTABLET, FILM COATED72
60760-736-60Famotidine60 in 1 BOTTLE, PLASTICTABLET, FILM COATED602

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60760-736-07EA - Each60760-7369be0b045-828c-4670-badc-de058084ef1c12023-04-07
60760-736-60EA - Each60760-7361f8681b9-386c-4d92-adef-1f69e04bdb5e12023-02-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60760-736FAMOTIDINE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY]2Current NDC, Legacy NDC, 2 package rows20230219_f175822d-7ca4-fa33-e053-2995a90ac310.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
284245famotidine 40 MG Oral TabletPSNf175822d-7ca4-fa33-e053-2995a90ac3102
284245famotidine 40 MG Oral TabletSCDf175822d-7ca4-fa33-e053-2995a90ac3102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
60760-736-07607600736077 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-736-07) 2023-02-06NoNoCurrent
60760-736-606076007366060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-736-60) 2022-12-080000-00-00NoNoCurrent