Maximum Strength Zantac description, usages, side effects, indications, overdosage, supplying and lots more!

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Maximum Strength Zantac

Boehringer Ingelheim Pharmaceuticals Inc.
Boehringer Ingelheim Pharmaceuticals Inc.




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet) Purpose
Ranitidine 150 mg (as ranitidine hydrochloride 168 mg)...................................................................................................... Acid reducer
  • 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

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

• 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
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.

  • 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
  • Blister: do not use if individual blister unit is open or torn
    Bottle: do not use if printed foil under bottle cap is open or torn
  • store at 20º-25ºC (68º-77ºF)
  • avoid excessive heat or humidity
  • this product is sodium and sugar free

hypromellose, magnesium stearate, microcrystalline cellulose, synthetic red iron oxide, titanium dioxide, triacetin

Call 1-888-285-9159 or visit www.zantacotc.com

Uses

Zantac 150mg – Blister Pack
NDC: 0597–0121–24

Maximum Strength Zantac

Zantac 150mg – 65ct. Bottle
NDC: 0597–0121–64

Maximum Strength Zantac

Maximum Strength Zantac

ranitidine TABLET, COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0597-0121
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
RANITIDINE HYDROCHLORIDE RANITIDINE 150 mg

Inactive Ingredients

Ingredient Name Strength
HYPROMELLOSES
MAGNESIUM STEARATE
cellulose, microcrystalline
ferric oxide red
titanium dioxide
triacetin

Product Characteristics

Color Size Imprint Code Shape
PINK (Dark Pink) 4 mm Z;150 PENTAGON (5 sided)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3 in 1 BLISTER PACK
2 50 in 1 BOTTLE
3 NDC:0597-0121-08 1 in 1 POUCH
4 8 in 1 BLISTER PACK
5 65 in 1 BOTTLE
6 1 in 1 POUCH
7 45 in 1 BOTTLE
8 85 in 1 BOTTLE
9 NDC:0597-0121-85 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021698 2006-12-21


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