NDC 65862-535 – Amoxicillin and Clavulanate Potassium

Amoxicillin 600 mg/5mL; Clavulanate Potassium 42.9 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug

Product NDC65862-535

Product details

Brand name
Amoxicillin and Clavulanate Potassium
Generic name
Amoxicillin and Clavulanate Potassium
Labeler
Aurobindo Pharma Limited
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA201091
Marketed since
December 20, 2011
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 (3)

Package NDCDescriptionSince
65862-535-02200 mL in 1 BOTTLE (65862-535-02)Dec 20, 2011
65862-535-13125 mL in 1 BOTTLE (65862-535-13)Dec 20, 2011
65862-535-7575 mL in 1 BOTTLE (65862-535-75)Dec 20, 2011

Other amoxicillin and clavulanate potassium products