FAMOTIDINE - famotidine tablet, film coated 
CVS Pharmacy, Inc.

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Drug Facts

Active ingredient (in each tablet)

Famotidine USP 20 mg

Purpose

Acid reducer

Uses


Warnings


Allergy alert: Do not use if you are allergic to famotidine or other acid reducers

Do not use


Ask a doctor before use if you have


Ask a doctor or pharmacist before use if you are

taking a prescription drug. Acid reducers may interact with certain prescription drugs.

Stop use and ask a doctor if


If pregnant or breast-feeding,


ask a health professional before use.

Keep out of reach of children.


In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions



Other information


Inactive ingredients


carnauba wax, corn starch, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, red iron oxide, sodium starch glycolate, talc, titanium dioxide and yellow iron oxide.

Questions or comments?


call 1-855-274-4122

Tips for Managing Heartburn

 



JUST ONE TABLET prevents and relieves heartburn due to acid indigestion brought on by eating and drinking certain foods and beverages.

Do not use if carton is open or if printed foil seal under bottle cap is open or torn.

Distributed by:
CVS Pharmacy, Inc.
One CVS Drive
Woonsocket, RI 02895
© 2023 CVS/pharmacy
CVS.com®
1-800-SHOP CVS

Made in India        V-33009
Code: TS/DRUGS/22/2009

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL -20 mg (25 Tablets, Container Label)

♥CVS
Health®

NDC 69842-087-53


MAXIMUM STRENGTH

Acid Controller
FAMOTIDINE
TABLETS USP 20 mg
Acid reducer

25 TABLETS
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL -20 mg (25 Tablets, Container Label)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL -20 mg (25 Tablets, Container Carton Label)

♥CVS
Health®

Compare to the active ingredient
in Maximum Strength Pepcid® AC*
NDC 69842-087-53

MAXIMUM STRENGTH

Acid
Controller
FAMOTIDINE TABLETS
USP 20 mg
Acid reducer

Just one tablet:
Prevents & relieves heartburn
due to acid indigestion

Actual Size

Package Contains
One Bottle

25 TABLETS
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL -20 mg (25 Tablets, Container Carton Label)






FAMOTIDINE 
famotidine tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-087
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FAMOTIDINE (UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) FAMOTIDINE20 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX (UNII: R12CBM0EIZ)  
STARCH, CORN (UNII: O8232NY3SJ)  
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
Product Characteristics
ColorYELLOWScoreno score
ShapeROUND (Square shaped Biconvex) Size5mm
FlavorImprint Code CC;59
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-087-531 in 1 CARTON02/03/2020
125 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:69842-087-141 in 1 CARTON02/03/2020
250 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:69842-087-211 in 1 CARTON02/03/2020
3100 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:69842-087-802 in 1 CARTON01/25/2021
4100 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:69842-087-791 in 1 CARTON12/01/2022
58 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20653102/03/2020
Labeler - CVS Pharmacy, Inc. (062312574)
Registrant - Aurohealth LLC (078728447)
Establishment
NameAddressID/FEIBusiness Operations
APL HEALTHCARE LIMITED650844777ANALYSIS(69842-087) , MANUFACTURE(69842-087)
Establishment
NameAddressID/FEIBusiness Operations
Aurobindo Pharma Limited650381903ANALYSIS(69842-087) , MANUFACTURE(69842-087)

Revised: 11/2023
Document Id: fe9a2cc4-b5bc-4941-a4a1-040f4c5393bd
Set id: 479a1437-a212-49d9-b272-758c0e5b7203
Version: 8
Effective Time: 20231116
 
CVS Pharmacy, Inc.