Cefaclor 500 mg/1
Cefaclor · TABLET, FILM COATED, EXTENDED RELEASE · Teva Pharmaceuticals USA, Inc.
Cefaclor is a tablet, film coated, extended release containing cefaclor at 500 mg/1, taken oral. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- Cefaclor
- Generic Name
- Cefaclor
- NDC Code (Product)
0093-1087- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA065058
- Marketing Start
- 09/26/2002
Recall History
No Recall HistoryFrequently Asked Questions
What is Cefaclor used for?
Cefaclor contains Cefaclor. It is a tablet, film coated, extended release taken oral. Consult your doctor for specific uses.
Is Cefaclor a controlled substance?
Cefaclor is not classified as a controlled substance by the DEA.
What is the generic name for Cefaclor?
The generic name for Cefaclor is Cefaclor. There are no other listed brand versions of Cefaclor.
What is the NDC code for Cefaclor 500 mg/1?
The NDC (National Drug Code) for Cefaclor 500 mg/1 is 0093-1087, listed by Teva Pharmaceuticals USA, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)