NDC 0093-3109 – Amoxicillin

Amoxicillin 500 mg/1 · Capsule · Oral

Human Prescription Drug 4 recalls

Product NDC0093-3109

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA061926
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 (2)

Package NDCDescriptionSince
0093-3109-05500 CAPSULE in 1 BOTTLE (0093-3109-05)Sep 30, 1990
0093-3109-5350 CAPSULE in 1 BOTTLE (0093-3109-53)Sep 30, 1990

Recalls mentioning this NDC

Other Amoxicillin products