NDC 81964-220 – Amoxicillin and Clavulanate Potassium
Amoxicillin 562.5 mg/1; Clavulanate Potassium 62.5 mg/1; Amoxicillin Sodium 437.5 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC81964-220
Product details
- Brand name
- Amoxicillin and Clavulanate Potassium
- Generic name
- Amoxicillin and clavulanate potassium
- Labeler
- USAntibiotics, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA050785
- Marketed since
- December 15, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Penicillin-class Antibacterial; Penicillin-class Antibacterial; beta Lactamase Inhibitor
Active ingredients
- Amoxicillin 562.5 mg/1
- Clavulanate Potassium 62.5 mg/1
- Amoxicillin Sodium 437.5 mg/1
Uses, dosage, side effects and warnings for Amoxicillin and clavulanate potassium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 81964-220-28 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-28) | Dec 15, 2025 |
| 81964-220-40 | 40 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-40) | Dec 15, 2025 |
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