NDC 0781-1874 – Amoxicillin and Clavulanate Potassium

Amoxicillin 250 mg/1; Clavulanate Potassium 125 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC0781-1874

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 · ANDA065189
Marketed since
August 23, 2005
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 (1)

Package NDCDescriptionSince
0781-1874-3130 TABLET, FILM COATED in 1 BOTTLE (0781-1874-31)Aug 23, 2005

Recalls mentioning this NDC

Other Amoxicillin and clavulanate potassium products