NDC 0781-6104 – Amoxicillin and Clavulanate Potassium

Amoxicillin 400 mg/5mL; Clavulanate Potassium 57 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug 1 recall

Product NDC0781-6104

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

Uses, dosage, side effects and warnings for Amoxicillin and clavulanate potassium →

Package NDC codes (3)

Package NDCDescriptionSince
0781-6104-46100 mL in 1 BOTTLE (0781-6104-46)Jun 5, 2002
0781-6104-5250 mL in 1 BOTTLE (0781-6104-52)Dec 18, 2023
0781-6104-5775 mL in 1 BOTTLE (0781-6104-57)Dec 18, 2023

Recalls mentioning this NDC

Other Amoxicillin and clavulanate potassium products