ZANTAC 360- famotidine tablet, film coated 
Select Corporation

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Zantac 360°™

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 right away (1-800-222-1222).

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, yellow iron oxide

Questions or Comments?

call 1-800-633-1610 or visit www.zantacotc.com

Product Repackaged and Distributed
with permission of manufacturer by:
Select Corporation Carrollton, TX 75007

PRINCIPAL DISPLAY PANEL - 1 Tablet Pouch Blister Pack

NEW FORMULA
MAXIMUM STRENGTH
See New Warnings

Zantac
360°
Famotidine Tablets USP 20 mg/Acid Reducer

JUST ONE TABLET
PREVENTS
& RELIEVES
HEARTBURN
DUE TO ACID
INDIGESTION

1 TABLET
Actual Size

2111926095.A

Principal Display Panel - 1 Tablet Pouch Blister Pack
ZANTAC 360 
famotidine tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52904-926(NDC:41167-0360)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
famotidine (UNII: 5QZO15J2Z8) (famotidine - UNII:5QZO15J2Z8) famotidine10 mg
Inactive Ingredients
Ingredient NameStrength
carnauba wax (UNII: R12CBM0EIZ)  
STARCH, CORN (UNII: O8232NY3SJ)  
magnesium stearate (UNII: 70097M6I30)  
microcrystalline cellulose (UNII: OP1R32D61U)  
ferric oxide red (UNII: 1K09F3G675)  
talc (UNII: 7SEV7J4R1U)  
titanium dioxide (UNII: 15FIX9V2JP)  
hydroxypropyl cellulose (1600000 WAMW) (UNII: RFW2ET671P)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
hypromellose 2910 (5 mpa.s) (UNII: R75537T0T4)  
Product Characteristics
ColorPINKScoreno score
ShapeROUND (biconvex) Size5mm
FlavorImprint Code CC;58
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52904-926-041 in 1 BLISTER PACK04/12/2021
11 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20653104/12/2021
Labeler - Select Corporation (053805599)

Revised: 4/2022
Document Id: 2332d799-0c86-4b40-b0f8-9571bdfe266e
Set id: 228b4c42-eef3-45c9-b48d-cbfb9d816c54
Version: 1
Effective Time: 20220413
 
Select Corporation