RANITIDINE 75- ranitidine tablets usp, 75mg tablet 
The Kroger Co.

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Drug Facts

Active ingredient (in each tablet)

Ranitidine 75 mg (as ranitidine hydrochloride, USP 84 mg)

Purpose

Acid reducer

Uses

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

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 Breat Feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep Out of Reach of Children.

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.

Question Section

Questions? call 1-888-375-3784

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

Package Label Principal Display Panel

Ranitidine Tablets USP, 75 mg - container label

container

Ranitidine Tablets USP, 75 mg - Container carton label

Ranitidine Tablets USP, 75 mg - Container carton label

containercarton

RANITIDINE 75 
ranitidine tablets usp, 75mg tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-131(NDC:55111-131)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ranitidine hydrochloride (UNII: BK76465IHM) (ranitidine - UNII:884KT10YB7) ranitidine75 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSES (UNII: 3NXW29V3WO)  
magnesium stearate (UNII: 70097M6I30)  
cellulose, microcrystalline (UNII: OP1R32D61U)  
Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
Ferrosoferric Oxide (UNII: XM0M87F357)  
titanium dioxide (UNII: 15FIX9V2JP)  
Product Characteristics
ColorPINKScoreno score
ShapeROUNDSize7mm
FlavorImprint Code P75
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-131-301 in 1 CARTON03/31/201109/30/2019
130 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:30142-131-601 in 1 CARTON03/31/201109/30/2019
260 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07529403/31/2011
Labeler - The Kroger Co. (006999528)

Revised: 9/2019
Document Id: 601f58c2-9b1b-961b-1f23-2c0d7a885604
Set id: 9589228d-1c1e-7a81-b64d-e9ca6a141a8b
Version: 5
Effective Time: 20190930
 
The Kroger Co.