NDC 68788-8759 – Amoxicillin

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

Human Prescription Drug

Product NDC68788-8759

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA065322
Marketed since
October 17, 2024
Listing expires
December 31, 2027
Pharmacologic class
Penicillin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Amoxicillin →

Package NDC codes (1)

Package NDCDescriptionSince
68788-8759-1150 mL in 1 BOTTLE (68788-8759-1)Oct 17, 2024

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