Ranitidine 75 description, usages, side effects, indications, overdosage, supplying and lots more!

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Ranitidine 75

REMEDYREPACK INC.

Major Pharmaceuticals Ranitidine 75 Tablets Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

OTC - ACTIVE INGREDIENT

Ranitidine 75 mg (as ranitidine hydrochloride 84 mg)

 

OTC - PURPOSE

Acid reducer

 

INDICATIONS & USAGE

  • 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

 

  • 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

 

  • 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

 

  • your heartburn continues or worsens
  • you need to take this product for more than 14 days

 

ask a health professional before use.

 

In case of overdose, get medical help or contact a Poison Control Center right away.

 

DOSAGE & ADMINISTRATION

  • 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

 

STORAGE AND HANDLING

  • do not use if printed foil under cap is broken or missing
  • store at 20° - 25°C (68° - 77°F)
  • avoid excessive heat or humidity
  • this product is sugar free

 

INACTIVE INGREDIENT

colloidal silicon dioxide, croscarmellose sodium, diethyl phthalate, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose, titanium dioxide.

 

OTC - QUESTIONS

1-800-719-9260

 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION

DRUG: Ranitidine 75


GENERIC: Ranitidine


DOSAGE: TABLET


ADMINSTRATION: ORAL


NDC: 52125-719-02


ACTIVE INGREDIENT(S):

  • RANITIDINE HYDROCHLORIDE 75mg in 1


COLOR: pink


SHAPE: HEXAGON (6 sided)


SCORE: No score


SIZE: 8 mm


IMPRINT: W75


PACKAGING: 30 in 1 BLISTER PACK



Ranitidine 75

Ranitidine 75

Ranitidine 75

Ranitidine TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:52125-719(NDC:0904-5818)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
RANITIDINE HYDROCHLORIDE RANITIDINE 75 mg

Product Characteristics

Color Size Imprint Code Shape
pink 8 mm W75 HEXAGON (6 sided)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52125-719-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076760 2013-09-26


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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