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

Menu
Search

Ranitidine

Shasun Pharmaceuticals Limited
Shasun Pharmaceuticals Limited

Ranitidine Tablet USP, 75 mg


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient (in each tablet)

Ranitidine 75 mg (as ranitidine hydrochloride 84 mg)

Purpose

Acid reducer

Ranitidine 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

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

Ranitidine Other information

●    Blister: do not use if individual blister unit is open or torn

       Bottle: do not use of printed foil under bottle cap is open or torn

●    store at 20°-25°C (68°-77°F)

●    avoid excessive heat or humidity

●    this product is sodium and sugar free

Inactive ingredients

Colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, talc, titanium dioxide.

Questions?

call 1-800-406-7984

IMPORTANT

Read the directions, consumer information leaflet and warnings before use. It contains important information.

Distributed by: Ohm Laboratories Inc, 1385 Livingston Avenue, North Brunsluick, NJ 08902

MADE IN INDIA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ranitidine

Ranitidine

Ranitidine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57910-405
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
RANITIDINE HYDROCHLORIDE RANITIDINE 75 mg

Inactive Ingredients

Ingredient Name Strength
COLLOIDAL SILICON DIOXIDE
CROSCARMELLOSE SODIUM
HYPROMELLOSES
ferric oxide red
MAGNESIUM STEARATE
cellulose, microcrystalline
polyethylene glycol 400
talc
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
PINK 8 mm OR;606 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57910-405-34 12000 in 1 BAG

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA201745 2012-02-29


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.