NDC 0093-7172-01
Etodolac 500 mg/1
Etodolac · TABLET, FILM COATED, EXTENDED RELEASE
Etodolac is a tablet, film coated, extended release containing etodolac at a strength of 500 mg/1. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- Etodolac
- Generic Name
- Etodolac
- NDC Code (Package)
0093-7172-01- NDC Code (Product)
0093-7172- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA075665
- Drug Class
- Nonsteroidal Anti-inflammatory Drug [EPC]
- Marketing Start
- 08/11/2000
Recall History
No Recall HistoryView Full Drug Page
Etodolac — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.