Sunmark Acid Reducer Maximum Strength

Generic Name: ranitidine hydrochloride
Dosage Form: tablet

McKesson Acid Reducer Drug Facts

Active ingredient (in each tablet)

Ranitidine 150 mg (as ranitidine hydrochloride 168 mg)

Slideshow: 2014 Update - First Time Brand-to-Generic Switches

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 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 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 cap is broken or missing (Bottle Only)
  • do not use if blister unit is broken or torn (Blister Only)
  • avoid excessive heat or humidity
  • store at 20° - 25°C (68° - 77°F)
  • this product is sugar free

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, diethyl phthalate, FD&C yellow #6, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose and titanium dioxide.

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to Zantac 150® Active Ingredient

Ranitidine Tablets, 150 mg

Acid Reducer

Prevents and Relieves Heartburn Associated with Acid Indigestion and Sour Stomach

Maximum Strength

(# Doses) {Replace "#" with the number of tablets in the package}

Acid Reducer Carton

SUNMARK ACID REDUCER  MAXIMUM STRENGTH
ranitidine tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49348-850
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RANITIDINE HYDROCHLORIDE (RANITIDINE) RANITIDINE 150 mg
Product Characteristics
Color ORANGE Score no score
Shape HEXAGON (6 sided) Size 11mm
Flavor Imprint Code W;741
Contains         
Packaging
# Item Code Package Description
1 NDC:49348-850-54 1 BOTTLE (BOTTLE) in 1 CARTON
1 65 TABLET (TABLET) in 1 BOTTLE
2 NDC:49348-850-04 3 BLISTER PACK (BLISTER PACK) in 1 CARTON
2 8 TABLET (TABLET) in 1 BLISTER PACK
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078653 02/13/2008
Labeler - McKesson (177667227)
Revised: 05/2009
 
McKesson



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