Major Heartburn Relief

Product NDC
0904-5780
11-digit product format
009045780
Labeler code
0904
Product ID
0904-5780_2b99e188-08ce-4160-bf19-136bc4dd39be
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA077351
Marketing category
ANDA
Marketing start
2006-09-29
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
Major Heartburn Relief
Brand name suffix
Maximum Strength
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
0904-5780-17Major Heartburn ReliefMaximum Strength1 in 1 BLISTER PACKTABLET, FILM COATED18
0904-5780-17Major Heartburn ReliefMaximum Strength25 in 1 CARTONTABLET, FILM COATED258
0904-5780-51Major Heartburn ReliefMaximum Strength50 in 1 BOTTLETABLET, FILM COATED508
0904-5780-51Major Heartburn ReliefMaximum Strength1 in 1 CARTONTABLET, FILM COATED18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0904-5780MAJOR HEARTBURN RELIEF MAXIMUM STRENGTH (FAMOTIDINE) TABLET, FILM COATED [MAJOR PHARMACEUTICALS]8Current NDC, Legacy NDC, 4 package rows20250209_ee0a263e-3f78-4534-9a30-803de636f92b.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310273famotidine 20 MG Oral TabletPSNee0a263e-3f78-4534-9a30-803de636f92b8
310273famotidine 20 MG Oral TabletSCDee0a263e-3f78-4534-9a30-803de636f92b8

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0904-5780-170090457801725 BLISTER PACK in 1 CARTON (0904-5780-17) / 1 TABLET, FILM COATED in 1 BLISTER PACK25 blister pack2006-10-040000-00-00NoNoCurrent
0904-5780-51009045780511 BOTTLE in 1 CARTON (0904-5780-51) / 50 TABLET, FILM COATED in 1 BOTTLE1 bottle2006-09-290000-00-00NoNoCurrent