NDC 0781-6102 – Amoxicillin and Clavulanate Potassium
Amoxicillin 200 mg/5mL; Clavulanate Potassium 28.5 mg/5mL · Powder, For Suspension · Oral
Product NDC0781-6102
Product details
- Brand name
- Amoxicillin and Clavulanate Potassium
- Generic name
- Amoxicillin and Clavulanate Potassium
- Labeler
- Sandoz Inc
- Dosage form
- Powder, For Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA065066
- Marketed since
- June 5, 2002
- Listing expires
- December 31, 2026
- Pharmacologic class
- Penicillin-class Antibacterial; beta Lactamase Inhibitor
Active ingredients
- Amoxicillin 200 mg/5mL
- Clavulanate Potassium 28.5 mg/5mL
Uses, dosage, side effects and warnings for Amoxicillin and clavulanate potassium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0781-6102-46 | 100 mL in 1 BOTTLE (0781-6102-46) | Jun 5, 2002 |
| 0781-6102-52 | 50 mL in 1 BOTTLE (0781-6102-52) | May 15, 2024 |
| 0781-6102-57 | 75 mL in 1 BOTTLE (0781-6102-57) | Dec 18, 2023 |
Recalls mentioning this NDC
- D-0868-2017 Jun 7, 2017 · Class III
Subpotent Drug; Clavulanic Acid
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