NDC 0093-4155 – Amoxicillin

Amoxicillin 250 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug 4 recalls

Product NDC0093-4155

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA061931
Marketed since
September 30, 1990
Listing expires
December 31, 2026
Pharmacologic class
Penicillin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Amoxicillin →

Package NDC codes (3)

Package NDCDescriptionSince
0093-4155-73100 mL in 1 BOTTLE (0093-4155-73)Sep 30, 1990
0093-4155-7980 mL in 1 BOTTLE (0093-4155-79)Sep 30, 1990
0093-4155-80150 mL in 1 BOTTLE (0093-4155-80)Sep 30, 1990

Recalls mentioning this NDC

Other Amoxicillin products