Nateglinide 120 mg/1
Nateglinide · TABLET, COATED · Cadila Pharmaceuticals Limited
No Recall History
Plain English
Nateglinide is a tablet, coated containing nateglinide at 120 mg/1, taken oral. Manufactured by Cadila Pharmaceuticals Limited.
Key Facts
- Brand Name
- Nateglinide
- Generic Name
- Nateglinide
- NDC Code (Product)
71209-031- Manufacturer
- Cadila Pharmaceuticals Limited
- Strength
- 120 mg/1
- Dosage Form
- TABLET, COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA206432
- Drug Class
- Glinide [EPC]
- Marketing Start
- 02/10/2014
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
blood glucose increased76 reports
diarrhoea65 reports
drug ineffective65 reports
dyspnoea64 reports
fatigue58 reports
nausea57 reports
renal failure51 reports
death48 reports
decreased appetite47 reports
vomiting44 reports
Frequently Asked Questions
What is Nateglinide used for?
Nateglinide contains Nateglinide. It is a tablet, coated taken oral. Consult your doctor for specific uses.
Is Nateglinide a controlled substance?
Nateglinide is not classified as a controlled substance by the DEA.
What is the generic name for Nateglinide?
The generic name for Nateglinide is Nateglinide. There are 2 other brand versions of Nateglinide.
What is the NDC code for Nateglinide 120 mg/1?
The NDC (National Drug Code) for Nateglinide 120 mg/1 is 71209-031, listed by Cadila Pharmaceuticals Limited.