NDC 71205-712 – Amoxicillin and Clavulanate Potassium

Amoxicillin 875 mg/1; Clavulanate Potassium 125 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-712

Product details

Brand name
Amoxicillin and Clavulanate Potassium
Generic name
Amoxicillin and Clavulanate Potassium
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065063
Marketed since
May 1, 2020
Listing expires
December 31, 2026
Pharmacologic class
Penicillin-class Antibacterial; beta Lactamase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Amoxicillin and clavulanate potassium →

Package NDC codes (8)

Package NDCDescriptionSince
71205-712-1010 TABLET, FILM COATED in 1 BOTTLE (71205-712-10)Nov 15, 2022
71205-712-1414 TABLET, FILM COATED in 1 BOTTLE (71205-712-14)Nov 15, 2022
71205-712-2020 TABLET, FILM COATED in 1 BOTTLE (71205-712-20)Nov 15, 2022
71205-712-2121 TABLET, FILM COATED in 1 BOTTLE (71205-712-21)Nov 15, 2022
71205-712-2828 TABLET, FILM COATED in 1 BOTTLE (71205-712-28)Nov 15, 2022
71205-712-3030 TABLET, FILM COATED in 1 BOTTLE (71205-712-30)Nov 15, 2022
71205-712-6060 TABLET, FILM COATED in 1 BOTTLE (71205-712-60)Nov 15, 2022
71205-712-9090 TABLET, FILM COATED in 1 BOTTLE (71205-712-90)Nov 15, 2022

Other Amoxicillin and clavulanate potassium products