NDC 0781-5061 – Amoxicillin

Amoxicillin 875 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 3 recalls

Product NDC0781-5061

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Sandoz Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065228
Marketed since
July 13, 2005
Listing expires
December 31, 2027
Pharmacologic class
Penicillin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Amoxicillin →

Package NDC codes (2)

Package NDCDescriptionSince
0781-5061-01100 TABLET, FILM COATED in 1 BOTTLE (0781-5061-01)Jul 13, 2005
0781-5061-2020 TABLET, FILM COATED in 1 BOTTLE (0781-5061-20)Jul 13, 2005

Recalls mentioning this NDC

Other Amoxicillin products