NDC 65862-503 – Amoxicillin and Clavulanate Potassium
Amoxicillin 875 mg/1; Clavulanate Potassium 125 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-503
Product details
- Brand name
- Amoxicillin and Clavulanate Potassium
- Generic name
- Amoxicillin and Clavulanate Potassium
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091568
- Marketed since
- January 20, 2012
- Listing expires
- December 31, 2027
- Pharmacologic class
- Penicillin-class Antibacterial; beta Lactamase Inhibitor
Active ingredients
- Amoxicillin 875 mg/1
- Clavulanate Potassium 125 mg/1
Uses, dosage, side effects and warnings for Amoxicillin and clavulanate potassium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 65862-503-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-503-01) | Jan 20, 2012 |
| 65862-503-20 | 20 TABLET, FILM COATED in 1 BOTTLE (65862-503-20) | Jan 20, 2012 |
Recalls mentioning this NDC
- D-0852-2020 Feb 19, 2020 · Class II
Presence of Foreign Substance: Customer complaint of a foreign substance identified as nylon cable tie
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