Skip to Content

← See all omeprazole brands

omeprazole by REMEDYREPACK INC.

Medically reviewed on May 15, 2017

Dosage form: tablet, delayed release
Ingredients: OMEPRAZOLE 20mg
Labeler: REMEDYREPACK INC.
NDC Code: 70518-0537

Perrigo Omeprazole Drug Facts

Active ingredient (in each tablet)

Omeprazole 20 mg

Purpose

Acid reducer

Uses
  • treats frequent heartburn (occurs 2 or more days a week)
  • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Warnings

Allergy alert: Do not use if you are allergic to omeprazole

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.

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

Ask a doctor or pharmacist before use if you are taking
  • warfarin, clopidogrel or cilostazol (blood-thinning medicines)
  • prescription antifungal or anti-yeast medicines
  • diazepam (anxiety medicine)
  • digoxin (heart medicine)
  • tacrolimus or mycophenolate mofetil (immune system medicines)
  • prescription antiretrovirals (medicines for HIV infection)
  • methotrexate (arthritis medicine)

Stop use and ask a doctor if
  • your heartburn continues or worsens
  • you need to take this product for more than 14 days
  • you need to take more than 1 course of treatment every 4 months
  • you get diarrhea

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
  • for adults 18 years of age and older
  • this product is to be used once a day (every 24 hours), every day for 14 days
  • it may take 1 to 4 days for full effect; some people get complete relief of symptoms within 24 hours

14-Day Course of Treatment

  • swallow 1 tablet with a glass of water before eating in the morning
  • take every day for 14 days
  • do not take more than 1 tablet a day
  • do not use for more than 14 days unless directed by your doctor
  • swallow whole. Do not chew or crush tablets

Repeated 14-Day Courses (if needed)

  • you may repeat a 14-day course every 4 months
  • do not take for more than 14 days or more often than every 4 months unless directed by a doctor
  • children under 18 years of age: ask a doctor. Heartburn in children may sometimes be caused by a serious condition.

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

Inactive ingredients

carnauba wax, ferric oxide red, ferric oxide yellow, hypromellose, hypromellose acetate succinate, lactose monohydrate, monoethanolamine, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, sodium stearate, sodium stearyl fumarate, talc, titanium dioxide, triethyl citrate

Questions or comments?

1-800-719-9260

DRUG: omeprazole

GENERIC: Omeprazole

DOSAGE: TABLET, DELAYED RELEASE

ADMINSTRATION: ORAL

NDC: 70518-0537-0

COLOR: brown

SHAPE: OVAL

SCORE: No score

SIZE: 17 mm

IMPRINT: 20

PACKAGING: 100 in 1 BOTTLE, PLASTIC

ACTIVE INGREDIENT(S):

  • OMEPRAZOLE 20mg in 1

INACTIVE INGREDIENT(S):

  • CARNAUBA WAX
  • SODIUM STEARYL FUMARATE
  • TALC
  • SODIUM STEARATE
  • TITANIUM DIOXIDE
  • TRIETHYL CITRATE
  • MONOETHANOLAMINE
  • FERRIC OXIDE RED
  • FERRIC OXIDE YELLOW
  • HYPROMELLOSES
  • LACTOSE MONOHYDRATE
  • PROPYLENE GLYCOL
  • SODIUM LAURYL SULFATE

OMEPRAZOLE 
omeprazole tablet, delayed release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70518-0537(NDC:45802-888)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OMEPRAZOLE (OMEPRAZOLE) OMEPRAZOLE20 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
FERRIC OXIDE RED 
FERRIC OXIDE YELLOW 
HYPROMELLOSES 
LACTOSE MONOHYDRATE 
PROPYLENE GLYCOL 
SODIUM LAURYL SULFATE 
SODIUM STEARATE 
SODIUM STEARYL FUMARATE 
TALC 
TITANIUM DIOXIDE 
TRIETHYL CITRATE 
MONOETHANOLAMINE 
Product Characteristics
ColorbrownScoreno score
ShapeOVALSize17mm
FlavorImprint Code20
Contains    
Packaging
#Item CodePackage Description
1NDC:70518-0537-0100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02203205/15/2017
Labeler - REMEDYREPACK INC. (829572556)

 
REMEDYREPACK INC.

← See all omeprazole brands

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide