acid reducer

Product NDC
69842-659
11-digit product format
698420659
Labeler code
69842
Product ID
69842-659_3f788e2f-ca72-48dc-9c29-866f5a6137c6
Type
HUMAN OTC DRUG
Nonproprietary name
famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
CVS Pharmacy
Application
ANDA077351
Marketing category
ANDA
Marketing start
2022-04-04
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
acid reducer
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
69842-659-63acid reducer25 in 1 BOTTLETABLET, FILM COATED253
69842-659-63acid reducer1 in 1 CARTONTABLET, FILM COATED13
69842-659-71acid reducer1 in 1 CARTONTABLET, FILM COATED13
69842-659-71acid reducer50 in 1 BOTTLETABLET, FILM COATED503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-659ACID REDUCER (FAMOTIDINE) TABLET, FILM COATED [CVS PHARMACY]3Current NDC, Legacy NDC, 4 package rows20250409_373f5e28-e9e2-4af7-8a27-29b5d8f28b50.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310273famotidine 20 MG Oral TabletPSN373f5e28-e9e2-4af7-8a27-29b5d8f28b503
310273famotidine 20 MG Oral TabletSCD373f5e28-e9e2-4af7-8a27-29b5d8f28b503

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-659-63698420659631 BOTTLE in 1 CARTON (69842-659-63) / 25 TABLET, FILM COATED in 1 BOTTLE1 bottle2022-04-040000-00-00NoNoCurrent
69842-659-71698420659711 BOTTLE in 1 CARTON (69842-659-71) / 50 TABLET, FILM COATED in 1 BOTTLE1 bottle2025-04-01NoNoHistorical