Famotidine

Product NDC
60687-595
11-digit product format
606870595
Labeler code
60687
Product ID
60687-595_22df1947-9de4-70ec-e063-6394a90a2077
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
American Health Packaging
Application
ANDA206530
Marketing category
ANDA
Marketing start
2021-03-09
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
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
FAMOTIDINE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5QZO15J2Z8
Rxcui310273

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
60687-595-01Famotidine100 in 1 BOX, UNIT-DOSETABLET, FILM COATED1004
60687-595-11Famotidine1 in 1 BLISTER PACKTABLET, FILM COATED14

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60687-595-01EA - Each60687-595a9e88907-559d-4a98-82bb-ec45a69c79d912021-02-05
60687-595-11EA - Each60687-595835a91df-2ab7-4836-8933-bb6d0e37626812021-02-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60687-595FAMOTIDINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]4Current NDC, Legacy NDC, 2 package rows20240926_3a583080-6771-4246-a221-2491e9e5d8af.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310273famotidine 20 MG Oral TabletPSN3a583080-6771-4246-a221-2491e9e5d8af4
310273famotidine 20 MG Oral TabletSCD3a583080-6771-4246-a221-2491e9e5d8af4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60687-595-0160687059501100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-595-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-595-11) 100 blister pack2021-03-090000-00-00NoNoCurrent
60687-595-11606870595111 in 1 BLISTER PACKHistorical