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

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FAMOTIDINE

Wockhardt USA LLC.

Famotidine Tablets, USP 20 mg


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION


Drugs Facts

Active ingredient (in each tablets)


Purpose


FAMOTIDINE 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 food and beverages

Warnings

Allergy alert: Do not use if you are allergic to famotidine 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.
  • if you have kidney disease, except under the advice and supervision of a doctor
  • with other acid reducers
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 dizziness
  • 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 a doctor if
  • your heartburn continues or worsens
  • you need to take this product for more than 14 days
If pregnant or breast-feeding,Keep out of reach of children.

Directions

  • adults and children 12 years and over:
  • to relieve symptoms, swallow 1 tablet with a glass of water. Do not chew.
  • to prevent symptoms, swallow 1 tablet with a glass of water at any time from 10 to 60 minutes before eating food or drinking beverages that cause heartburn
  • do not use more than 2 tablets in 24 hours
  • children under 12 years: ask a doctor

FAMOTIDINE Other information

  • read the directions and warnings before use
  • store at 20°-25°C (68°-77°F)
  • keep the carton. It contains important information.
  • protect from moisture

Inactive ingredients

Questions or comments?

1-800-346-6854

Manufactured by:



Distributed by:






FAMOTIDINE
FAMOTIDINE

FAMOTIDINE

FAMOTIDINE TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64679-374
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FAMOTIDINE FAMOTIDINE 20 mg

Inactive Ingredients

Ingredient Name Strength
cellulose, microcrystalline
STARCH, CORN
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED
talc
MAGNESIUM STEARATE
HYPROMELLOSE 2910 (6 MPA.S)
titanium dioxide
polyethylene glycol 400

Product Characteristics

Color Size Imprint Code Shape
white (white) 9 mm W374 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE
2 30 in 1 BOTTLE
3 500 in 1 BOTTLE
4 10 in 1 BLISTER PACK
5 NDC:64679-374-00 38000 in 1 DRUM
6 NDC:64679-374-09 6500 in 1 DRUM

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090837 2010-08-06


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