NDC 0093-8675 – Amoxicillin and Clavulanate Potassium
Amoxicillin 600 mg/5mL; Clavulanate Potassium 42.9 mg/5mL · Powder, For Suspension · Oral
Product NDC0093-8675
Product details
- Brand name
- Amoxicillin and Clavulanate Potassium
- Generic name
- Amoxicillin and Clavulanate Potassium
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Powder, For Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA065162
- Marketed since
- September 23, 2004
- Listing expires
- December 31, 2027
- Pharmacologic class
- Penicillin-class Antibacterial; beta Lactamase Inhibitor
Active ingredients
- Amoxicillin 600 mg/5mL
- Clavulanate Potassium 42.9 mg/5mL
Uses, dosage, side effects and warnings for amoxicillin and clavulanate potassium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0093-8675-74 | 200 mL in 1 BOTTLE (0093-8675-74) | Sep 23, 2004 |
| 0093-8675-75 | 125 mL in 1 BOTTLE (0093-8675-75) | Sep 23, 2004 |
| 0093-8675-78 | 75 mL in 1 BOTTLE (0093-8675-78) | Sep 23, 2004 |
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