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Ranitidine 150 by Walmart Stores Inc.

Dosage form: tablet, coated
Ingredients: RANITIDINE HYDROCHLORIDE 150mg
Labeler: Walmart Stores Inc.
NDC Code: 49035-404

Drug Facts

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 eating or drinking certain foods and beverages

Warnings

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

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 diziness
  • 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

Stop use and ask 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.

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

  • do not use if printed foil under bottle cap is open or torn
  • store at 20°-25°C (68°-77°F)
  • avoid excessive heat or humidity
  • protect from light
  • this product is sodium and sugar free

Inactive ingredients

FD&C red #40 aluminum lake, hypromellose, iron oxide black, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide

Questions

Call 1-888-287-1915

TAMPER EVIDENT: DO NOT USE IF FOIL SEAL UNDER CAP PRINTED WITH "SEALED FOR YOUR PROTECTION" IS BROKEN OR MISSING

IMPORTANT: Read the directions, consumer information leaflet and warnings before use. Keep the carton. It contains important information.

Ranitidine Tablets, 150 mg 24 count Carton

NDC 49035-404-34

equate

Compare to
Maximum
Strength
Zantac 150®
Tablets Active
Ingredient*

Maximum Strength

Ranitidine
Tablets, 150 mg

Acid Reducer

  • PREVENTS AND
    RELIEVES
    HEARTBURN
    associated with
    acid indigestion
    and sour stomach

150 mg 24 TABLETS (24 DOSES)

Ranitidine Tablets, 150 mg 24 count Bottle

equate™ NDC 49035-404-34

Maximum Strength

Ranitidine
Tablets, 150 mg

Acid Reducer

  • PREVENTS AND RELIEVES
    HEARTBURN
    associated
    with acid
    indigestion
    and sour
    stomach

150 mg 24 TABLETS (24 DOSES)

RANITIDINE 150 
ranitidine hydrochloride tablets 150mg tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-404(NDC:55111-404)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RANITIDINE HYDROCHLORIDE (RANITIDINE) RANITIDINE150 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 
HYPROMELLOSE 2910 (6 MPA.S) 
FERROSOFERRIC OXIDE 
magnesium stearate 
cellulose, microcrystalline 
POLYETHYLENE GLYCOL 400 
titanium dioxide 
Product Characteristics
ColorPINKScoreno score
ShapeROUNDSize9mm
FlavorImprint CodeR150
Contains    
Packaging
#Item CodePackage Description
1NDC:49035-404-341 BOTTLE in 1 CARTON
124 TABLET, COATED in 1 BOTTLE
2NDC:49035-404-611 BOTTLE in 1 CARTON
265 TABLET, COATED in 1 BOTTLE
3NDC:49035-404-132 BOTTLE in 1 CARTON
365 TABLET, COATED in 1 BOTTLE
4NDC:49035-404-651 BOTTLE in 1 CARTON
4220 TABLET, COATED in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07819201/05/2010
Labeler - Walmart Stores Inc. (051957769)

 
Walmart Stores Inc.

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Medically reviewed on May 24, 2018

Further information

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

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