NDC 0143-9889 – Amoxicillin

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

Human Prescription Drug

Product NDC0143-9889

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA065322
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
0143-9889-01100 mL in 1 BOTTLE (0143-9889-01)Jun 19, 2006
0143-9889-15150 mL in 1 BOTTLE (0143-9889-15)Jun 19, 2006
0143-9889-8080 mL in 1 BOTTLE (0143-9889-80)Jun 19, 2006

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