Sumatriptan and Naproxen Sodium 500 mg/1
Sumatriptan and Naproxen Sodium · TABLET, FILM COATED · Sun Pharmaceutical Industries, Inc.
Sumatriptan and Naproxen Sodium is a tablet, film coated containing sumatriptan and naproxen sodium at 500 mg/1, taken oral. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Sumatriptan and Naproxen Sodium
- Generic Name
- Sumatriptan and Naproxen Sodium
- NDC Code (Product)
47335-410- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA202803
- Marketing Start
- 07/20/2018
Recall History
No Recall HistoryFrequently Asked Questions
What is Sumatriptan and Naproxen Sodium used for?
Sumatriptan and Naproxen Sodium contains Sumatriptan and Naproxen Sodium. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Sumatriptan and Naproxen Sodium a controlled substance?
Sumatriptan and Naproxen Sodium is not classified as a controlled substance by the DEA.
What is the generic name for Sumatriptan and Naproxen Sodium?
The generic name for Sumatriptan and Naproxen Sodium is Sumatriptan and Naproxen Sodium. There are no other listed brand versions of Sumatriptan and Naproxen Sodium.
What is the NDC code for Sumatriptan and Naproxen Sodium 500 mg/1?
The NDC (National Drug Code) for Sumatriptan and Naproxen Sodium 500 mg/1 is 47335-410, listed by Sun Pharmaceutical Industries, Inc..
Other Sumatriptan and Naproxen Sodium Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)