NDC 76420-859 – Amoxicillin and Clavulanate Potassium

Amoxicillin 200 mg/5mL; Clavulanate Potassium 28.5 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug

Product NDC76420-859

Product details

Brand name
Amoxicillin and Clavulanate Potassium
Generic name
Amoxicillin and Clavulanate Potassium
Labeler
Asclemed USA, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA201090
Marketed since
December 20, 2011
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
76420-859-01100 mL in 1 BOTTLE (76420-859-01)Oct 24, 2024
76420-859-5050 mL in 1 BOTTLE (76420-859-50)Oct 24, 2024
76420-859-7575 mL in 1 BOTTLE (76420-859-75)Oct 24, 2024

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