Ranitidine 150: Package Insert and Label Information

RANITIDINE 150- ranitidine hydrochloride tablet, coated
Walmart Stores Inc.

cartonbottle

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)

carton
(click image for full-size original)

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)

bottle
(click image for full-size original)

RANITIDINE 150 ranitidine hydrochloride tablets 150mg tablet, coated
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-404(NDC:55111-404)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RANITIDINE HYDROCHLORIDE (RANITIDINE) RANITIDINE 150 mg
Inactive Ingredients
Ingredient Name Strength
FD&C RED NO. 40
HYPROMELLOSE 2910 (6 MPA.S)
FERROSOFERRIC OXIDE
magnesium stearate
cellulose, microcrystalline
POLYETHYLENE GLYCOL 400
titanium dioxide
Product Characteristics
Color PINK Score no score
Shape ROUND Size 9mm
Flavor Imprint Code R150
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49035-404-34 1 BOTTLE in 1 CARTON contains a BOTTLE
1 24 TABLET, COATED in 1 BOTTLE This package is contained within the CARTON (49035-404-34)
2 NDC:49035-404-61 1 BOTTLE2 BOTTLE in 1 CARTON contains a BOTTLE
2 NDC:49035-404-13 1 BOTTLE2 BOTTLE in 1 CARTON contains a BOTTLE
2 65 TABLET, COATED in 1 BOTTLE This package is contained within a CARTON (49035-404-61) and a CARTON (49035-404-13)
3 NDC:49035-404-65 1 BOTTLE in 1 CARTON contains a BOTTLE
3 220 TABLET, COATED in 1 BOTTLE This package is contained within the CARTON (49035-404-65)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078192 01/05/2010
Labeler — Walmart Stores Inc. (051957769)

Revised: 05/2018 Walmart Stores Inc.

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