NDC 0781-1831 – Amoxicillin and Clavulanate Potassium
Amoxicillin 500 mg/1; Clavulanate Potassium 125 mg/1 · Tablet, Film Coated · Oral
Product NDC0781-1831
Product details
- Brand name
- Amoxicillin and Clavulanate Potassium
- Generic name
- Amoxicillin and Clavulanate Potassium
- Labeler
- Sandoz Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA065064
- Marketed since
- March 15, 2002
- Listing expires
- December 31, 2026
- Pharmacologic class
- Penicillin-class Antibacterial; beta Lactamase Inhibitor
Active ingredients
- Amoxicillin 500 mg/1
- Clavulanate Potassium 125 mg/1
Uses, dosage, side effects and warnings for Amoxicillin and clavulanate potassium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0781-1831-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-1831-01) | Sep 20, 2022 |
| 0781-1831-13 | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0781-1831-13) | Mar 15, 2002 |
| 0781-1831-20 | 20 TABLET, FILM COATED in 1 BOTTLE (0781-1831-20) | Mar 15, 2002 |
Recalls mentioning this NDC
- D-0868-2017 Jun 7, 2017 · Class III
Subpotent Drug; Clavulanic Acid
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