NDC 71205-035 – Amoxicillin

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

Human Prescription Drug

Product NDC71205-035

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065228
Marketed since
July 13, 2005
Listing expires
December 31, 2026
Pharmacologic class
Penicillin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Amoxicillin →

Package NDC codes (5)

Package NDCDescriptionSince
71205-035-1414 TABLET, FILM COATED in 1 BOTTLE (71205-035-14)Sep 1, 2019
71205-035-2020 TABLET, FILM COATED in 1 BOTTLE (71205-035-20)May 1, 2018
71205-035-3030 TABLET, FILM COATED in 1 BOTTLE (71205-035-30)May 1, 2018
71205-035-6060 TABLET, FILM COATED in 1 BOTTLE (71205-035-60)May 1, 2018
71205-035-9090 TABLET, FILM COATED in 1 BOTTLE (71205-035-90)May 1, 2018

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