NDC 62135-089 – Amoxicillin

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

Human Prescription Drug

Product NDC62135-089

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Chartwell RX, LLC
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA061931
Marketed since
September 30, 1990
Listing expires
December 31, 2027
Pharmacologic class
Penicillin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Amoxicillin →

Package NDC codes (3)

Package NDCDescriptionSince
62135-089-01100 mL in 1 BOTTLE (62135-089-01)Jul 16, 2026
62135-089-51150 mL in 1 BOTTLE (62135-089-51)Jul 16, 2026
62135-089-8080 mL in 1 BOTTLE (62135-089-80)Jul 16, 2026

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