NDC 0143-9887 – Amoxicillin

Amoxicillin 400 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug 1 recall

Product NDC0143-9887

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA065325
Marketed since
June 19, 2006
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
0143-9887-01100 mL in 1 BOTTLE (0143-9887-01)Jun 19, 2006
0143-9887-5050 mL in 1 BOTTLE (0143-9887-50)Jun 19, 2006
0143-9887-7575 mL in 1 BOTTLE (0143-9887-75)Jun 19, 2006

Recalls mentioning this NDC

Other Amoxicillin products