NDC 0781-6039 – Amoxicillin

Amoxicillin 125 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug 3 recalls

Product NDC0781-6039

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Sandoz Inc
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA065387
Marketed since
March 26, 2007
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
0781-6039-46100 mL in 1 BOTTLE (0781-6039-46)Mar 26, 2007
0781-6039-55150 mL in 1 BOTTLE (0781-6039-55)Mar 26, 2007
0781-6039-5880 mL in 1 BOTTLE (0781-6039-58)Mar 26, 2007

Recalls mentioning this NDC

Other Amoxicillin products