NDC 73043-009 – Amoxicillin and Clavulanate Potassium

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

Human Prescription Drug

Product NDC73043-009

Product details

Brand name
Amoxicillin and Clavulanate Potassium
Generic name
Amoxicillin and Clavulanate Potassium
Labeler
Devatis, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA210416
Marketed since
November 1, 2024
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
73043-009-0150 mL in 1 BOTTLE (73043-009-01)Nov 1, 2024
73043-009-0275 mL in 1 BOTTLE (73043-009-02)Nov 1, 2024
73043-009-03100 mL in 1 BOTTLE (73043-009-03)Nov 1, 2024

Other Amoxicillin and clavulanate potassium products