RANITIDINE- ranitidine tablet, coated 
Dr. Reddy's Laboratories Limited

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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

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
  • kidney disease

Ask a doctor or pharmacist before use if you are

• taking a prescription drug. Acid reducers may interact with certain prescription drugs.

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 (1-800-222-1222).

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

Read the directions and warnings before use. Keep the carton. It contains important information including tips for managing heartburn.

Tips for managing heartburn

Revised: 03/20

PACKAGE LABEL PRINCIPAL DISPLAY PANEL

Container Label:

Dr.Reddy's
NDC 55111-404-34


Maximum Strength
Ranitidine
Tablets USP,150 mg
ACID REDUCER


PREVENTS & RELIEVES
HEARTBURN associated with acid indigestion
and sour stomach

24 Tablets(24 doses)

container

Container Carton Label:

Dr.Reddy's
NDC 55111-404-34


Compare to the active
ingredient in Zantact 150® Tablets*


Maximum Strength
Ranitidine
Tablets USP,150 mg
ACID REDUCER


PREVENTS & RELIEVES
heartburn associated with acid indigestion
and sour stomach

24 Tablets(24 doses)


containercarton

Blister Carton Label:

Dr.Reddy's
NDC 55111-404-24


Maximum Strength
Ranitidine
Tablets USP,150 mg
ACID REDUCER


PREVENTS & RELIEVES
HEARTBURN associated with acid indigestion
and sour stomach

24 Tablets(24 doses)

blistercarton

RANITIDINE 
ranitidine tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)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:55111-404-341 in 1 CARTON12/02/2009
124 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:55111-404-321 in 1 CARTON12/02/2009
232 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:55111-404-361 in 1 CARTON12/02/2009
336 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:55111-404-501 in 1 CARTON12/02/2009
450 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:55111-404-611 in 1 CARTON12/02/2009
565 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:55111-404-552 in 1 CARTON01/05/2010
665 in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:55111-404-621 in 1 CARTON12/02/2009
795 in 1 BOTTLE; Type 0: Not a Combination Product
8NDC:55111-404-902 in 1 CARTON12/02/2009
895 in 1 BOTTLE; Type 0: Not a Combination Product
9NDC:55111-404-021 in 1 CARTON12/02/2009
9200 in 1 BOTTLE; Type 0: Not a Combination Product
10NDC:55111-404-651 in 1 CARTON12/02/2009
10220 in 1 BOTTLE; Type 0: Not a Combination Product
11NDC:55111-404-171 in 1 CARTON12/02/2009
118 in 1 BLISTER PACK; Type 0: Not a Combination Product
12NDC:55111-404-243 in 1 CARTON12/02/2009
128 in 1 BLISTER PACK; Type 0: Not a Combination Product
13NDC:55111-404-384 in 1 CARTON12/02/2009
138 in 1 BLISTER PACK; Type 0: Not a Combination Product
14NDC:55111-404-401 in 1 BOTTLE12/02/2009
1440 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07819212/02/2009
Labeler - Dr. Reddy's Laboratories Limited (650562841)

Revised: 4/2020
Document Id: 8459fe61-6721-7cfb-31a4-b05105bc73b8
Set id: 00df8a42-296f-80dd-98af-ee8b30eb38cc
Version: 11
Effective Time: 20200420
 
Dr. Reddy's Laboratories Limited