NDC 65862-503 – Amoxicillin and Clavulanate Potassium

Amoxicillin 875 mg/1; Clavulanate Potassium 125 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

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

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

Package NDC codes (2)

Package NDCDescriptionSince
65862-503-01100 TABLET, FILM COATED in 1 BOTTLE (65862-503-01)Jan 20, 2012
65862-503-2020 TABLET, FILM COATED in 1 BOTTLE (65862-503-20)Jan 20, 2012

Recalls mentioning this NDC

Other Amoxicillin and clavulanate potassium products