WAL-ZAN- ranitidine hydrochloride tablets 150mg tablet, coated 
Walgreens Company

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Drug Facts

Active ingredient (in each tablet)

Ranitidine 150 mg (as ranitidine hydrochloride USP, 168 mg)

Purpose

Acid reducer

Use(s)

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 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 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

Other information

Inactive ingredients

FD&C red #40 aluminum lake, hypromellose, iron oxide black, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide

Questions

call 1-888-375-3784

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.

container label

carton

WAL-ZAN 
ranitidine hydrochloride tablets 150mg tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0010(NDC:55111-404)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RANITIDINE HYDROCHLORIDE (UNII: BK76465IHM) (RANITIDINE - UNII:884KT10YB7) RANITIDINE150 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
magnesium stearate (UNII: 70097M6I30)  
cellulose, microcrystalline (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
titanium dioxide (UNII: 15FIX9V2JP)  
Product Characteristics
ColorPINKScoreno score
ShapeROUNDSize9mm
FlavorImprint Code R150
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0010-341 in 1 CARTON06/11/2011
124 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:0363-0010-501 in 1 CARTON06/11/2011
250 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:0363-0010-621 in 1 CARTON06/11/2011
395 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:0363-0010-321 in 1 CARTON06/11/2011
432 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:0363-0010-011 in 1 CARTON06/11/2011
5200 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:0363-0010-231 in 1 CARTON06/11/2011
636 in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:0363-0010-261 in 1 CARTON06/11/2011
765 in 1 BOTTLE; Type 0: Not a Combination Product
8NDC:0363-0010-611 in 1 CARTON06/11/2011
865 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07819206/11/2011
Labeler - Walgreens Company (008965063)

Revised: 11/2017
Document Id: 9b415007-a9fb-03b9-b8ec-5f96d120f040
Set id: 9f7d916b-1624-5cf6-2394-50a557c016ad
Version: 3
Effective Time: 20171107
 
Walgreens Company