up and up omeprazole 20 mg/1
Omeprazole · TABLET, DELAYED RELEASE · Target Corporation
up and up omeprazole is a tablet, delayed release containing omeprazole at 20 mg/1, taken oral. Manufactured by Target Corporation.
Key Facts
- Brand Name
- up and up omeprazole
- Generic Name
- Omeprazole
- NDC Code (Product)
11673-915- Manufacturer
- Target Corporation
- Strength
- 20 mg/1
- Dosage Form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA022032
- Drug Class
- Proton Pump Inhibitor [EPC]
- Marketing Start
- 07/14/2009
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Use • 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
Dosage & Administration
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.
Warnings
Warnings Allergy alert: • do not use if you are allergic to omeprazole. • omeprazole may cause severe skin reactions. Symptoms may include: • skin reddening • blisters • rash If an allergic reaction occurs, stop use and seek medical help right away. Do not use if you have: • trouble or pain swallowing food, vomiting with blood, or bloody or black stools • 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 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. • frequent wheezing, particularly with heartburn • unexplained weight loss • nausea or vomiting • stomach pain 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 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 • you d…
Frequently Asked Questions
What is up and up omeprazole used for?
up and up omeprazole contains Omeprazole. It is a tablet, delayed release taken oral. Consult your doctor for specific uses.
Is up and up omeprazole a controlled substance?
up and up omeprazole is not classified as a controlled substance by the DEA.
What is the generic name for up and up omeprazole?
The generic name for up and up omeprazole is Omeprazole. There are 11 other brand versions of Omeprazole.
What is the NDC code for up and up omeprazole 20 mg/1?
The NDC (National Drug Code) for up and up omeprazole 20 mg/1 is 11673-915, listed by Target Corporation.
Other Omeprazole Brands
See all →- Omeprazole20 mg/111673-948
- Omeprazole10 mg/116714-630
- Omeprazole and Sodium Bicarbonate40 mg/127241-032
- Good Sense Omeprazole20 mg/10113-0915
- Good Sense Omeprazole20 mg/10113-1723
- Acid Reducer20 mg/130142-077
- omeprazole20 mg/142507-164
- omeprazole20 mg/142507-414
- Omeprazole20 mg/142708-170
- Omeprazole20 mg/143063-743
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)