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

Human Prescription Drug

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

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

Package NDC codes (2)

Package NDCDescriptionSince
81964-220-2828 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-28)Dec 15, 2025
81964-220-4040 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-40)Dec 15, 2025

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