NDC 0093-8675 – Amoxicillin and Clavulanate Potassium

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

Human Prescription Drug

Product NDC0093-8675

Product details

Brand name
Amoxicillin and Clavulanate Potassium
Generic name
Amoxicillin and Clavulanate Potassium
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA065162
Marketed since
September 23, 2004
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
0093-8675-74200 mL in 1 BOTTLE (0093-8675-74)Sep 23, 2004
0093-8675-75125 mL in 1 BOTTLE (0093-8675-75)Sep 23, 2004
0093-8675-7875 mL in 1 BOTTLE (0093-8675-78)Sep 23, 2004

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