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 HistoryFrequently 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.
Product NDC
11673-915
Package NDCs (2)
- 11673-915-01
1 BOTTLE in 1 CARTON (11673-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- 11673-915-03
3 BOTTLE in 1 CARTON (11673-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
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)