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Heartburn Relief Maximum Strength

Medically reviewed on July 16, 2018

Dosage form: tablet, film coated
Ingredients: RANITIDINE HYDROCHLORIDE 150mg
Labeler: SUPERVALU INC.
NDC Code: 41163-062

Equaline 44-620-Delisted

Active ingredient (in each tablet)

Ranitidine 150 mg
(as ranitidine hydrochloride USP, 168 mg)

Purpose

Acid reducer

Uses
  • relieves heartburn associated with acid indigestion and sour stomach
  • prevents heartburn associated with acid indigestion and sour stomach brought on by certain foods and beverages 

Warnings

Allergy alert: Do not use if you are allergic to ranitidine or any 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
  • if you have kidney disease, except under the advice and supervision of a doctor 

Ask a doctor before use if you have
  • frequent chest pain
  • frequent wheezing, particularly with heartburn
  • unexplained weight loss
  • nausea or vomiting
  • stomach pain
  • 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

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:
    • to relieve symptoms, swallow 1 tablet with a glass of water
    • to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn
    • can be used up to twice daily (do not take more than 2 tablets in 24 hours)
  • children under 12 years: ask a doctor 

Other information
  • TAMPER EVIDENT: DO NOT USE IF THE CARTON OR INDIVIDUAL BLISTER UNIT IS OPEN OR TORN
  • store at 20º-25ºC (68º-77ºF)
  • avoid excessive heat or humidity
  • this product is sodium and sugar free
  • see end flap for expiration date and lot number 

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol, talc, titanium dioxide 

Questions or comments?

Call 1-877-932-7948 24 hours a day, 7 days a week

Principal display panel

equaline®

compare to Zantac 150® active ingredient*

NDC 41163-062-08

maximum strength
heartburn relief
ranitidine tablets USP,
150 mg acid reducer

PREVENTS & RELIEVES:
HEARTBURN associated with acid indigestion & sour stomach

24 tablets (24 doses)

TAMPER EVIDENT: DO NOT USE IF THE CARTON OR INDIVIDUAL BLISTER UNIT IS OPEN OR TORN

*This product is not manufactured or distributed by Boehringer Ingelheim Pharmaceuticals, Inc., owner of the registered trademark Zantac 150®.
50844    ORG031362008
Product of India

DISTRIBUTED BY SUPERVALU INC.
EDEN PRAIRIE, MN 55344 USA

We're committed to your satisfaction and guarantee the quality of this product. Contact us at 1-877-932-7948, or www.supervalu-ourownbrands.com.
Please have package available.

Equaline 44-620

HEARTBURN RELIEF  MAXIMUM STRENGTH
ranitidine tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-062
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RANITIDINE HYDROCHLORIDE (RANITIDINE) RANITIDINE150 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE 
CROSCARMELLOSE SODIUM 
HYPROMELLOSES 
FERRIC OXIDE RED 
MAGNESIUM STEARATE 
TALC 
TITANIUM DIOXIDE 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOLS 
Product Characteristics
ColorPINKScoreno score
ShapeOVALSize12mm
FlavorImprint Code9R
Contains    
Packaging
#Item CodePackage Description
1NDC:41163-062-083 BLISTER PACK in 1 CARTON
18 TABLET, FILM COATED in 1 BLISTER PACK
2NDC:41163-062-151 BOTTLE in 1 CARTON
250 TABLET, FILM COATED in 1 BOTTLE
3NDC:41163-062-651 BOTTLE in 1 CARTON
365 TABLET, FILM COATED in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20053606/15/201307/15/2018
Labeler - SUPERVALU INC. (006961411)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(41163-062)
Establishment
NameAddressID/FEIOperations
Shasun Pharmaceuticals Limited915786829API MANUFACTURE(41163-062)

 
SUPERVALU INC.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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