good sense acid reducer

Product NDC
0113-0141
11-digit product format
001130141
Labeler code
0113
Product ID
0113-0141_78b30bf8-0525-4256-a2b4-7ca6efb78ada
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
L. Perrigo Company
Application
ANDA075400
Marketing category
ANDA
Marketing start
2009-10-23
Substance
FAMOTIDINE
Active strength
10 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
good sense acid reducer
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FAMOTIDINE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5QZO15J2Z8
Rxcui199047

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
0113-0141-65good sense acid reducer30 in 1 CARTONTABLET, FILM COATED306
0113-0141-65good sense acid reducer1 in 1 BLISTER PACKTABLET, FILM COATED16
0113-0141-75good sense acid reducer1 in 1 CARTONTABLET, FILM COATED16
0113-0141-90good sense acid reducer90 in 1 BOTTLETABLET, FILM COATED906

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0113-0141-65EA - Each0113-0141e617c6d2-4c26-49dd-ad33-8322d67726b812013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FAMOTIDINEACTIVE INGREDIENT5QZO15J2Z8GOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
FAMOTIDINEACTIVE MOIETY5QZO15J2Z8GOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675GOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
FERRIC OXIDE YELLOWINACTIVE INGREDIENTEX438O2MRTGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30GOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
POLYDEXTROSEINACTIVE INGREDIENTVH2XOU12IEGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
POLYETHYLENE GLYCOLINACTIVE INGREDIENT3WJQ0SDW1AGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
TALCINACTIVE INGREDIENT7SEV7J4R1UGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPGOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1
TRIACETININACTIVE INGREDIENTXHX3C3X673GOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET [L PERRIGO COMPANY]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0113-0141GOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET, FILM COATED [L. PERRIGO COMPANY]5Current NDC, Legacy NDC, 4 package rows20250212_cc77f6ff-a534-4731-b971-491280840899.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199047famotidine 10 MG Oral TabletPSNcc77f6ff-a534-4731-b971-4912808408996
199047famotidine 10 MG Oral TabletSCDcc77f6ff-a534-4731-b971-4912808408996

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0113-0141-650011301416530 BLISTER PACK in 1 CARTON (0113-0141-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK30 blister pack2009-10-230000-00-00NoNoCurrent
0113-0141-75001130141751 BOTTLE in 1 CARTON (0113-0141-75) / 90 TABLET, FILM COATED in 1 BOTTLE (0113-0141-90)1 bottle2026-05-140Current
0113-0141-900011301419090 in 1 BOTTLEHistorical