MAXIMUM STRENGTH ACID REDUCER- famotidine tablet 
TARGET CORPORATION

----------

Target Famotidine Tablets USP, 20 mg

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

  • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
  • with other acid reducers

Ask a doctor before use if you have

  • had heartburn over 3 months. This may be a sign of a more serious condition.
  • heartburn with lightheadedness, sweating, or dizziness
  • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
  • frequent chest pain
  • frequent wheezing, particularly with heartburn
  • unexplained weight loss
  • nausea or vomiting
  • stomach pain
  • kidney disease

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

  • your heartburn continues or worsens
  • you need to take this product for more than 14 days

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

adults and children 12 years and over:

children under 12 years: ask a doctor

Other information

Inactive ingredients carnauba wax, colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, pregelatinized starch, talc, titanium dioxide

Questions or comments? Call 1-800-910-6874

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

Tips for Managing Heartburn

famotidine-20mg-200s-labelfamotidine-20mg-200s-ifcfamotidine-20mg-100s-ifcfamotidine-20mg-50s-labelfamotidine-20mg-50s-ifcfamotidine-20mg-25ct-ifc

MAXIMUM STRENGTH ACID REDUCER 
famotidine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-697
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FAMOTIDINE (UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) FAMOTIDINE20 mg
Inactive Ingredients
Ingredient NameStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
MICROCRYSTALLINE CELLULOSE 102 (UNII: PNR0YF693Y)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
Product Characteristics
ColorwhiteScoreno score
ShapeSEMI-CIRCLE (D-shaped) Size9mm
FlavorImprint Code 87
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-697-525 in 1 CARTON05/15/2024
15 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:11673-697-051 in 1 CARTON05/15/2024
250 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:11673-697-012 in 1 CARTON05/15/2024
350 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:11673-697-201 in 1 CARTON05/15/2024
4200 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21754305/15/2024
Labeler - TARGET CORPORATION (006961700)
Registrant - TIME CAP LABORATORIES, INC. (037052099)
Establishment
NameAddressID/FEIBusiness Operations
MARKSANS PHARMA LIMITED925822975manufacture(11673-697)

Revised: 5/2024
Document Id: 18567eaf-6b97-8c6f-e063-6294a90a986d
Set id: 07a924f1-14cc-4e7d-e063-6394a90ac7f3
Version: 2
Effective Time: 20240513
 
TARGET CORPORATION